FDA Inspection
Fritz Huber MedizintechnikFritz Huber Medizintechnik – FDA Inspection, Jan 29, 2020
Record Details
This FDA Inspection record concerns Fritz Huber Medizintechnik, with an inspection on January 29, 2020, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Fritz Huber Medizintechnik
- Inspection Date
- January 29, 2020
- Product Type
- Devices
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ID · 0eb94f1a-d757-493a-9bbb-215f20d37307
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1116897
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
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Other FDA inspections of Fritz Huber Medizintechnik
1| Date | Classification | Office | Project area |
|---|---|---|---|
| June 25, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
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