FDA Inspection
Medikomp GmbhMedikomp Gmbh – FDA Inspection, Oct 20, 2016
Record Details
This FDA Inspection record concerns Medikomp Gmbh, with an inspection on October 20, 2016, issued by the Center for Devices and Radiological Health, covering devices.
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ID · c32bd902-b668-4c05-b045-a85cc32ce894
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 992713
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Medikomp Gmbh
2| Date | Classification | Office | Project area |
|---|---|---|---|
| May 14, 2025 | NAI | Compliance: Devices | |
| August 15, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Medikomp Gmbh
- FDA Inspection 1273889 - 2025-05-14
- FDA Inspection 849117 - 2013-08-15
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