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FDA Inspection
•CooperVision, Inc.•July 21, 2009

FDA Inspection 598905 - CooperVision, Inc. - July 21, 2009

Record Details

This FDA Inspection record concerns CooperVision, Inc., with an inspection on July 21, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company
CooperVision, Inc.
Inspection Date
July 21, 2009
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 6a3f8ce9-d317-4018-83ea-2f2b0bcf8bd3

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
598905
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of CooperVision, Inc.

3
DateClassificationOfficeProject area
April 11, 2018VAICenter for Devices and Radiological HealthCompliance: Devices
May 29, 2012NAICenter for Devices and Radiological HealthBioresearch Monitoring
October 24, 2011OAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for CooperVision, Inc.
  • FDA Inspection 1047905 - 2018-04-11
  • FDA Inspection 783764 - 2012-05-29
  • FDA Inspection 751853 - 2011-10-24

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