# FDA Inspection 680230 - Generic Medical Devices, Inc. - September 09, 2010

Source: https://www.keypedia.com/records/fda_inspections/generic-medical-devices-inc/aa82375e-d2ae-48a8-9c66-be0e16c3430a
Source feed: FDA_Inspections

> FDA inspection 680230 of Generic Medical Devices, Inc., September 09, 2010. Classification: Official Action Indicated (OAI). 6 citations under 21 CFR parts 803 and 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 680230
- Company Name: Generic Medical Devices, Inc.
- Inspection Date: 2010-09-09
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- [FDA Inspection 780253 - 2012-04-25](https://www.keypedia.com/records/fda_inspections/generic-medical-devices-inc/c3e74b81-c373-415f-adb9-ec755bff6848)

Company: https://www.keypedia.com/companies/generic-medical-devices-inc/0654a836-8a8d-4071-b3cc-b868c8458a63

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