FDA Inspection
PAR Medizintechnik GmbH & Co. KGPAR Medizintechnik GmbH & Co. KG – FDA Inspection, Jan 21, 2015
Record Details
This FDA Inspection record concerns PAR Medizintechnik GmbH & Co. KG, with an inspection on January 21, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- January 21, 2015
- Product Type
- Devices
View Company Profile
ID · 6e904c85-d363-45c7-b9e6-78eec4b38a41
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 913845
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 803.17(a)(2)Lack of System for Determining MDR Events
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Other FDA inspections of PAR Medizintechnik GmbH & Co. KG
1| Date | Classification | Office | Project area |
|---|---|---|---|
| January 16, 2025 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
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