FDA Inspection
Technolas Perfect Vision GmbHTechnolas Perfect Vision GmbH – FDA Inspection, Dec 9, 2010
Record Details
This FDA Inspection record concerns Technolas Perfect Vision GmbH, with an inspection on December 9, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- December 9, 2010
- Product Type
- Devices
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ID · 8a7582fd-ad77-4081-8a13-94a34dc5baa7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 702560
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
3- 21 CFR 820.25(b)Training records
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 803.17Lack of Written MDR Procedures
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Other FDA inspections of Technolas Perfect Vision GmbH
2| Date | Classification | Office | Project area |
|---|---|---|---|
| September 4, 2019 | Not classified | Office of Inspections and Investigations | |
| July 23, 2009 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Technolas Perfect Vision GmbH
- FDA Inspection 1124007 - 2019-09-04
- FDA Inspection 597702 - 2009-07-23
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