FDA Inspection
Nesher Pharmaceuticals (USA) LLCNesher Pharmaceuticals (USA) LLC – FDA Inspection, Dec 6, 2012
Record Details
This FDA Inspection record concerns Nesher Pharmaceuticals (USA) LLC, with an inspection on December 6, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- December 6, 2012
- Product Type
- Drugs
View Company Profile
ID · f1bb62cb-ac31-44b4-86fe-7493bd445131
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 811545
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Nesher Pharmaceuticals (USA) LLC
4| Date | Classification | Office | Project area |
|---|---|---|---|
| May 7, 2015 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 11, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 20, 2010 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 2, 2009 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Nesher Pharmaceuticals (USA) LLC
- FDA Inspection 925360 - 2015-05-07
- FDA Inspection 709386 - 2011-02-11
- FDA Inspection 677260 - 2010-08-20
- FDA Inspection 554856 - 2009-02-02
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