What is GP-12 Inspection?

What is GP-12 Inspection?

What is GP-12 Inspection? A Complete Breakdown for Automotive Suppliers | PTI

What is GP-12 Inspection? A Complete Breakdown for Automotive Suppliers

The **GP-12 Early Production Containment** standard is non-negotiable for automotive suppliers launching new parts. Understand the scope, timing, and non-compliance risks of the critical **GP-12 quality** process.

In the world of Tier 1 and Tier 2 automotive supply, quality is measured in defects per million, and launch periods are the most vulnerable time. To mitigate the risk of quality escapes during ramp-up, OEMs established mandatory containment protocols. The most common and stringent of these is **GP-12 inspection**.

If you are launching a new part, tool, or production process, understanding the mechanics of **GP-12** is essential to avoid costly, reputation-damaging violations.

Defining GP-12 Early Production Containment

GP-12 (Global Procedure 12) is an OEM-mandated quality standard requiring the supplier to implement a rigorous, heightened **quality inspection** and containment process during the early stages of production. Its core purpose is to validate that the supplier’s production control plan and quality systems are robust enough to consistently produce conforming parts.

The Purpose of GP-12

  • Defect Proofing: To quickly detect and contain any latent defects that may not have been found during the initial PPAP (Production Part Approval Process).
  • Process Validation: To confirm that all changes, including operator instructions, tooling, and gauges, are effective under real-world, high-volume production conditions.
  • Protecting the OEM: To prevent contaminated inventory from reaching the customer’s assembly line, thereby protecting brand reputation and avoiding costly line shutdowns.

When Is GP-12 Inspection Required?

GP-12 is not a one-time event; it is a time-bound and volume-specific requirement triggered by specific conditions:

Mandatory GP-12 Triggers

  1. New Product Launch (Mandatory): Any new part number going into production for the first time.
  2. New Tooling or Equipment: Introduction of new, modified, or transferred tooling used to produce existing parts.
  3. New Production Location: Moving production of an existing part to a new manufacturing plant.
  4. Significant Process Change: Any major change to the manufacturing process or sub-component sourcing that could impact final product quality.

Generally, the GP-12 containment period runs for a predetermined duration (often **30 days**) or a specified **minimum production volume**, whichever is met last. Successful completion requires 30 days of consecutive defect-free shipments.

The Scope of GP-12 Containment

The standard requires a **100% inspection** of all specified characteristics on every part shipped during the GP-12 period. This inspection must be separate and independent from the standard final inspection process.

Key Elements of GP-12 Implementation

Dedicated Inspection Area

A physically segregated and clearly labeled inspection area is mandatory. This space must be stocked with boundary samples and clear **work instructions** to prevent contamination with un-inspected inventory.

Data Tracking and Reporting

Every defect found must be logged and immediately communicated. The data—defect type, quantity, and time of discovery—is essential for the supplier to drive quick **root cause analysis** and Corrective Actions (PCAs).

Independent Personnel

While internal staff can perform the check, using **third-party quality inspection** services is highly recommended. An unbiased, certified team reduces operator fatigue bias and provides an external layer of validation to the OEM.

Exit Requirements

The supplier must demonstrate sustained conformance for the required duration/volume. The final **GP-12 sign-off** confirms the production process is validated and the heightened containment can be lifted.

The Risk of Non-Compliance

Failing to implement or sustain an effective GP-12 process can lead to immediate and severe consequences:

  • Elevated Containment (CS1/CS2): If a quality escape occurs during GP-12, the OEM will likely escalate the mandate to Controlled Shipping Level 1 (CS1) or even Controlled Shipping Level 2 (CS2), resulting in massive cost recovery fees.
  • Loss of Future Business: A GP-12 failure damages the supplier’s quality rating and can result in disqualification from future sourcing opportunities.
  • Costly Scrappage and Rework: Defects caught by the OEM result in charges for line downtime, emergency containment, and the cost of the faulty parts.

Effective GP-12 implementation is the best insurance policy during the critical launch phase, turning an obligation into a competitive advantage.

Need Immediate GP-12 Support or Inspection?

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