FDA Inspection
Recipharm Stockhom ABRecipharm Stockhom AB – FDA Inspection, Sep 13, 2011
Record Details
This FDA Inspection record concerns Recipharm Stockhom AB, with an inspection on September 13, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Recipharm Stockhom AB
- Inspection Date
- September 13, 2011
- Product Type
- Drugs
View Company Profile
ID · 93c1fd01-1789-457d-a7de-251b1eb02701
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 751078
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
1- 21 CFR 211.166(a)Written program not followed
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Other FDA inspections of Recipharm Stockhom AB
1| Date | Classification | Office | Project area |
|---|---|---|---|
| March 11, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Recipharm Stockhom AB
- FDA Inspection 874918 - 2014-03-11
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