FDA Inspection
Oculus Optikgeraete GMBHOculus Optikgeraete GMBH – FDA Inspection, Jun 24, 2010
Record Details
This FDA Inspection record concerns Oculus Optikgeraete GMBH, with an inspection on June 24, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Oculus Optikgeraete GMBH
- Inspection Date
- June 24, 2010
- Product Type
- Devices
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ID · aa16ecc0-8ad8-4caf-94aa-fe6de3a25e41
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 675579
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.40(a)Document review, approval by designated individual
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Other FDA inspections of Oculus Optikgeraete GMBH
2| Date | Classification | Office | Project area |
|---|---|---|---|
| November 10, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 19, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Oculus Optikgeraete GMBH
- FDA Inspection 998293 - 2016-11-10
- FDA Inspection 853199 - 2013-09-19
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