FDA Inspection
Rudolf Riester GmbhRudolf Riester Gmbh – FDA Inspection, Jun 24, 2010
Record Details
This FDA Inspection record concerns Rudolf Riester Gmbh, with an inspection on June 24, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Rudolf Riester Gmbh
- Inspection Date
- June 24, 2010
- Product Type
- Devices
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ID · f21bf988-64cd-41fa-a29e-94ce36f8f8c3
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 672689
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
4- 21 CFR 820.25(b)Training records
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.90(a)Nonconforming product control
- 21 CFR 820.70(i)Software validation for automated processes
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Other FDA inspections of Rudolf Riester Gmbh
1| Date | Classification | Office | Project area |
|---|---|---|---|
| May 16, 2019 | Not classified | Office of Inspections and Investigations |
Other documents for Rudolf Riester Gmbh
- FDA Inspection 1101224 - 2019-05-16
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