FDA Inspection
Richard Wolf GmbHRichard Wolf GmbH – FDA Inspection, Mar 6, 2024
Record Details
This FDA Inspection record concerns Richard Wolf GmbH, with an inspection on March 6, 2024, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
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ID · 85ecdb5c-cde8-439d-961b-4edc66f8a152
Inspection Facts
- Inspection number
- 1231967
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
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 |
|---|---|---|---|
| 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 |
| June 10, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Richard Wolf GmbH
- FDA Inspection 1198730 - 2022-10-20
- FDA Inspection 1106603 - 2019-09-10
- FDA Inspection 896070 - 2014-08-29
- FDA Inspection 665977 - 2010-06-10
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