FDA Inspection
Raritan Pharmaceuticals, Inc.Raritan Pharmaceuticals, Inc. – FDA Inspection, Sep 19, 2012
Record Details
This FDA Inspection record concerns Raritan Pharmaceuticals, Inc., with an inspection on September 19, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- September 19, 2012
- Product Type
- Drugs
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ID · af765194-be49-48aa-836e-424e9af61645
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 799355
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
1- 21 CFR 211.192Investigations of discrepancies, failures
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| August 21, 2012 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
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