FDA Inspection
Ciba Vision GmbHCiba Vision GmbH – FDA Inspection, Jun 30, 2011
Record Details
This FDA Inspection record concerns Ciba Vision GmbH, with an inspection on June 30, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Ciba Vision GmbH
- Inspection Date
- June 30, 2011
- Product Type
- Devices
View Company Profile
ID · e7637f69-0269-449d-9c39-fbf046f56974
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 734697
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
3- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
- 21 CFR 820.70(a)Production processes
- 21 CFR 820.50(a)(3)Acceptable supplier records, inadequate records
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Other FDA inspections of Ciba Vision GmbH
2| Date | Classification | Office | Project area |
|---|---|---|---|
| February 3, 2023 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 30, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Ciba Vision GmbH
- FDA Inspection 1198725 - 2023-02-03
- FDA Inspection 942005 - 2015-07-30
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