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

Source: https://www.keypedia.com/records/fda_inspections/coopervision-inc/23caa731-3e5d-4b95-90ba-514c62bfd969
Source feed: FDA_Inspections

> FDA inspection 598905 of CooperVision, Inc., July 21, 2009. 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: 598905
- Company Name: CooperVision, Inc.
- Inspection Date: 2009-07-21
- 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 751853 - 2011-10-24](https://www.keypedia.com/records/fda_inspections/coopervision-inc/87464afd-d545-497b-b12b-d658fc350cbc)

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