# CooperVision, Inc. – FDA Inspection, Oct 3, 2008

Source: https://www.keypedia.com/records/fda_inspections/coopervision-inc/1963016b-df41-4cf3-9fda-87b6785dc944
Source feed: FDA_Inspections

> FDA inspection 542489 of CooperVision, Inc., October 03, 2008. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 542489
- Company Name: CooperVision, Inc.
- Inspection Date: 2008-10-03
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1169289 - 2022-05-04](https://www.keypedia.com/records/fda_inspections/coopervision-inc/84264b23-565f-4fc2-9d26-e9f10dd61e37)
- [FDA Inspection 1008069 - 2017-04-13](https://www.keypedia.com/records/fda_inspections/coopervision-inc/20746ce9-0419-47c1-a7ee-c101397b2cd5)
- FDA Inspection 752767 - 2011-11-21

Company: https://www.keypedia.com/companies/coopervision-inc/8a545065-828e-4cad-9327-a02b81ddfd16

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