FDA Inspection
Archimica S.p.AArchimica S.p.A – FDA Inspection, Apr 28, 2017
Record Details
This FDA Inspection record concerns Archimica S.p.A, with an inspection on April 28, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · b69db2c0-61bd-40d2-ac41-184c857cabde
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1013470
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Archimica S.p.A
5| Date | Classification | Office | Project area |
|---|---|---|---|
| June 15, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 13, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 21, 2017 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 25, 2014 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 8, 2011 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Archimica S.p.A
- FDA Inspection 1220541 - 2023-06-15
- FDA Inspection 1123733 - 2018-09-13
- FDA Inspection 1094988 - 2017-07-21
- FDA Inspection 900514 - 2014-09-25
- FDA Inspection 744980 - 2011-09-08
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