# FDA Inspection 751853 - CooperVision, Inc. - October 24, 2011

Source: https://www.keypedia.com/records/fda_inspections/coopervision-inc/b0680b77-bbf5-467c-84f9-0355670d4fda
Source feed: FDA_Inspections

> FDA inspection 751853 of CooperVision, Inc., October 24, 2011. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 751853
- Company Name: CooperVision, Inc.
- Inspection Date: 2011-10-24
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1047905 - 2018-04-11
- [FDA Inspection 783764 - 2012-05-29](https://www.keypedia.com/records/fda_inspections/coopervision-inc/95b42b13-2949-47dd-ba53-5bcc9fd28c6f)
- FDA Inspection 598905 - 2009-07-21

Company: https://www.keypedia.com/companies/coopervision-inc/061cc3b3-31b8-42b8-a3f1-dc2e3a19b90c

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7