FDA Inspection
Bieffe Medital SpABieffe Medital SpA – FDA Inspection, Sep 28, 2018
Record Details
This FDA Inspection record concerns Bieffe Medital SpA, with an inspection on September 28, 2018, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Company
- Bieffe Medital SpA
- Inspection Date
- September 28, 2018
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 99e7c618-e88d-42ea-aca7-ab4e0388b5ea
Inspection Facts
- Inspection number
- 1126215
- FDA center
- Medical Devices & Rad Health
- 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 |
| May 29, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| 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 1057424 - 2018-05-29
- FDA Inspection 945063 - 2015-09-22
- FDA Inspection 844005 - 2013-08-15
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