# FDA Inspection 823008 - Regene - March 13, 2013

Source: https://www.keypedia.com/records/fda_inspections/regene/c7b59b0d-820d-42cd-97ac-321870baa810
Source feed: FDA_Inspections

> FDA Inspection 823008 for Regene on March 13, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 823008
- Company Name: Regene
- Inspection Date: 2013-03-13
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/regene/668d33b3-0882-4027-ad90-8b34ec433f8c

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