# FDA Inspection 551820 - G P M, Inc - December 15, 2008

Source: https://www.keypedia.com/records/fda_inspections/g-p-m-inc/0d8c7521-0cf3-4cdf-9c80-d4db3d01c6cf
Source feed: FDA_Inspections

> FDA Inspection 551820 for G P M, Inc on December 15, 2008. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 551820
- Company Name: G P M, Inc
- Inspection Date: 2008-12-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/g-p-m-inc/f7ea2227-1f37-449f-be97-6483ba59a6ad

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7