FDA Inspection
Bieffe Medital SpABieffe Medital SpA – FDA Inspection, May 29, 2018
Record Details
This FDA Inspection record concerns Bieffe Medital SpA, with an inspection on May 29, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 15f9154b-0a35-437c-b061-47e77172dd41
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1057424
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Bieffe Medital SpA
6| Date | Classification | Office | Project area |
|---|---|---|---|
| November 17, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 28, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 28, 2018 | Not classified | Office of Inspections and Investigations | |
| September 22, 2015 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 15, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Bieffe Medital SpA
- FDA Inspection 1235890 - 2023-11-17
- FDA Inspection 1128816 - 2019-06-28
- FDA Inspection 1126215 - 2018-09-28
- FDA Inspection 945063 - 2015-09-22
- FDA Inspection 844005 - 2013-08-15
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