FDA Inspection
HIPP medical AGHIPP medical AG – FDA Inspection, Jul 11, 2013
Record Details
This FDA Inspection record concerns HIPP medical AG, with an inspection on July 11, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- HIPP medical AG
- Inspection Date
- July 11, 2013
- Product Type
- Devices
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ID · 3e248a69-4322-406b-84de-c1df97f7226a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 845588
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.70(a)Process control procedures
- 21 CFR 820.100(a)Lack of or inadequate procedures
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Other FDA inspections of HIPP medical AG
2| Date | Classification | Office | Project area |
|---|---|---|---|
| January 22, 2025 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 22, 2017 | Not classified | Office of Inspections and Investigations | Postmarket Assurance: Devices |
Other documents for HIPP medical AG
- FDA Inspection 1261902 - 2025-01-22
- FDA Inspection 1015199 - 2017-06-22
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