FDA Inspection
B. Braun Avitum AGB. Braun Avitum AG – FDA Inspection, Jun 18, 2015
Record Details
This FDA Inspection record concerns B. Braun Avitum AG, with an inspection on June 18, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- B. Braun Avitum AG
- Inspection Date
- June 18, 2015
- Product Type
- Devices
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ID · e8c5af60-42d2-4455-8811-5659acc09ea3
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 933674
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
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Other FDA inspections of B. Braun Avitum AG
3| Date | Classification | Office | Project area |
|---|---|---|---|
| April 23, 2026 | Not classified | Office of Inspections and Investigations | |
| February 22, 2018 | Not classified | Office of Inspections and Investigations | |
| June 17, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for B. Braun Avitum AG
- FDA Inspection 1316972 - 2026-04-23
- FDA Inspection 1055481 - 2018-02-22
- FDA Inspection 735246 - 2011-06-17
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