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FDA Inspection
•Ciba Vision Corporation•December 22, 2010

Ciba Vision Corporation – FDA Inspection, Dec 22, 2010

Record Details

This FDA Inspection record concerns Ciba Vision Corporation, with an inspection on December 22, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company
Ciba Vision Corporation
Inspection Date
December 22, 2010
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 1e8d8bce-e1c5-4052-9b55-89585a9b0cdb

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
703632
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

3
  1. 21 CFR 820.184DHR - not or inadequately maintained
  2. 21 CFR 820.100(b)Documentation
  3. 21 CFR 820.90(a)Nonconforming product control

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Ciba Vision Corporation

2
DateClassificationOfficeProject area
May 9, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
May 1, 2012NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Ciba Vision Corporation
  • FDA Inspection 834845 - 2013-05-09
  • FDA Inspection 778963 - 2012-05-01

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