FDA Inspection
RAUMEDIC - MUENCHBERGRAUMEDIC - MUENCHBERG – FDA Inspection, Nov 2, 2017
Record Details
This FDA Inspection record concerns RAUMEDIC - MUENCHBERG, with an inspection on November 2, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Person
- Kimberly Lewandowski-Walker (Issuing Officer)
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ID · 82c76c14-bb4a-43a9-a4ad-298c84eece88
Inspection Facts
- Inspection number
- 1031821
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.30(g)Design validation - Risk analysis
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Other FDA inspections of RAUMEDIC - MUENCHBERG
2| Date | Classification | Office | Project area |
|---|---|---|---|
| February 2, 2023 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 29, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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