# 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 for Generic Medical Devices, Inc. on September 09, 2010. Classification: Official Action Indicated (OAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 780253 - 2012-04-25](https://www.keypedia.com/records/fda_inspections/generic-medical-devices-inc/2af40b34-2fae-4afd-94d6-937b87094df3)
- [FDA Inspection 680230 - 2010-09-09](https://www.keypedia.com/records/fda_inspections/generic-medical-devices-inc/edc22a28-b951-456a-beca-8eda6bbae107)

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