FDA Inspection
Unit Pack Company IncUnit Pack Company Inc – FDA Inspection, Oct 11, 2012
Record Details
This FDA Inspection record concerns Unit Pack Company Inc, with an inspection on October 11, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Unit Pack Company Inc
- Inspection Date
- October 11, 2012
- Product Type
- Drugs
View Company Profile
ID · b097db4c-3b79-4621-a710-40091d900834
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 802704
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
3- 21 CFR 211.188(b)(2)Identity of major equipment and lines used
- 21 CFR 211.160(b)(1)Samples (various types) representative, identified properly
- 21 CFR 211.192No written record of investigation
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Other FDA inspections of Unit Pack Company Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| December 9, 2015 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| October 26, 2009 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Unit Pack Company Inc
- FDA Inspection 953347 - 2015-12-09
- FDA Inspection 623551 - 2009-10-26
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