# FDA Inspection 561875 - GMR Products, Inc. - October 09, 2008

Source: https://www.keypedia.com/records/fda_inspections/gmr-products-inc/d807cafc-44e7-495b-81f6-5322cbb84f13
Source feed: FDA_Inspections

> FDA Inspection 561875 for GMR Products, Inc. on October 09, 2008. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 561875
- Company Name: GMR Products, Inc.
- Inspection Date: 2008-10-09
- 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/gmr-products-inc/4c8b7cb2-f357-4838-9e1f-5f623eb21a60

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