FDA Inspection
AllerganAllergan – FDA Inspection, Aug 22, 2012
Record Details
This FDA Inspection record concerns Allergan, with an inspection on August 22, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Allergan
- Inspection Date
- August 22, 2012
- Product Type
- Devices
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ID · 73fa9295-e120-4378-b2ee-086ebe6fea96
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 800575
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 812.40Sponsors" general responsibilities
- 21 CFR 812.140(b)(2)Sponsor device disposition records inadequate
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Other FDA inspections of Allergan
2| Date | Classification | Office | Project area |
|---|---|---|---|
| February 6, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 12, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Allergan
- FDA Inspection 865086 - 2014-02-06
- FDA Inspection 740227 - 2011-08-12
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