FDA Inspection
Richard Wolf GmbHRichard Wolf GmbH – FDA Inspection, Jun 10, 2010
Record Details
This FDA Inspection record concerns Richard Wolf GmbH, with an inspection on June 10, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Richard Wolf GmbH
- Inspection Date
- June 10, 2010
- Product Type
- Devices
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ID · 2f2b857b-e3fb-455d-98bc-ecf0c193afdc
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 665977
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.120(d)Records, DHR {see also 820.184(e)}
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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 |
| September 10, 2019 | VAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| August 29, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Richard Wolf GmbH
- FDA Inspection 1231967 - 2024-03-06
- FDA Inspection 1198730 - 2022-10-20
- FDA Inspection 1106603 - 2019-09-10
- FDA Inspection 896070 - 2014-08-29
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