FDA Inspection
E P Evans Drugs IncE P Evans Drugs Inc – FDA Inspection, Dec 16, 2013
Record Details
This FDA Inspection record concerns E P Evans Drugs Inc, with an inspection on December 16, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- E P Evans Drugs Inc
- Inspection Date
- December 16, 2013
- Product Type
- Drugs
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ID · 7e807dc8-5516-44fd-8371-9a0d0eafa2b5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 860321
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
6- 21 CFR 211.137(a)Expiration date lacking
- 21 CFR 211.82(b)Quarantine Storage of Components
- 21 CFR 211.125(f)Procedures Written and Followed
- 21 CFR 211.68(a)Written calibration / inspection records not kept
- 21 CFR 211.84(d)(1)Identity Testing of Each Component
- 21 CFR 211.80(a)Procedures To Be in Writing
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