FDA Inspection
Actavis Totowa LLCActavis Totowa LLC – FDA Inspection, Mar 31, 2009
Record Details
This FDA Inspection record concerns Actavis Totowa LLC, with an inspection on March 31, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Actavis Totowa LLC
- Inspection Date
- March 31, 2009
- Product Type
- Drugs
View Company Profile
ID · 437e9773-8d02-4864-ab3b-da7c6034101f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 563376
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
4- 21 CFR 211.84(b)Representative Samples
- 21 CFR 211.22(d)Procedures not in writing, fully followed
- 21 CFR 211.166(a)Written program not followed
- 21 CFR 211.80(a)Procedures To Be in Writing
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Other FDA inspections of Actavis Totowa LLC
2| Date | Classification | Office | Project area |
|---|---|---|---|
| June 3, 2010 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 3, 2010 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Actavis Totowa LLC
- FDA Inspection 665944 - 2010-06-03
- FDA Inspection 649153 - 2010-02-03
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