FDA Inspection
Hocoma AGHocoma AG – FDA Inspection, Jul 11, 2024
Record Details
This FDA Inspection record concerns Hocoma AG, with an inspection on July 11, 2024, issued by the Center for Devices and Radiological Health, covering devices.
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ID · c2db049d-c038-4a27-a0b3-2352ccdd8bad
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1245475
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
1- 21 CFR 820.90(b)(2)Product rework procedures, Lack of or inadequate procedures
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Other FDA inspections of Hocoma AG
1| Date | Classification | Office | Project area |
|---|---|---|---|
| December 7, 2017 | Not classified | Office of Inspections and Investigations |
Other documents for Hocoma AG
- FDA Inspection 1036878 - 2017-12-07
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