FDA Inspection
Richard Wolf GmbHRichard Wolf GmbH – FDA Inspection, Sep 10, 2019
Record Details
This FDA Inspection record concerns Richard Wolf GmbH, with an inspection on September 10, 2019, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 68725905-ad59-4fe9-abb8-eedbb7c26be6
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1106603
- FDA center
- Medical Devices & Rad Health
- Project area
- Radiation Control and Health Safety Act
Other FDA inspections of Richard Wolf GmbH
4| Date | Classification | Office | Project area |
|---|---|---|---|
| March 6, 2024 | Not classified | Office of Inspections and Investigations | Compliance: Devices |
| October 20, 2022 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 29, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 10, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Richard Wolf GmbH
- FDA Inspection 1231967 - 2024-03-06
- FDA Inspection 1198730 - 2022-10-20
- FDA Inspection 896070 - 2014-08-29
- FDA Inspection 665977 - 2010-06-10
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