FDA Inspection
FIS - Fabbrica Italiana Sintetici SpAFIS - Fabbrica Italiana Sintetici SpA – FDA Inspection, Feb 7, 2013
Record Details
This FDA Inspection record concerns FIS - Fabbrica Italiana Sintetici SpA, with an inspection on February 7, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- February 7, 2013
- Product Type
- Drugs
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ID · 8abb7677-5669-4315-a4fd-ba3d774e5d83
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 819321
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of FIS - Fabbrica Italiana Sintetici SpA
4| Date | Classification | Office | Project area |
|---|---|---|---|
| October 28, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 5, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 25, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 22, 2010 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for FIS - Fabbrica Italiana Sintetici SpA
- FDA Inspection 1276304 - 2022-10-28
- FDA Inspection 1110921 - 2019-07-05
- FDA Inspection 961470 - 2016-02-25
- FDA Inspection 650141 - 2010-01-22
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