# CooperVision, Inc. – FDA Inspection, Apr 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/coopervision-inc/20746ce9-0419-47c1-a7ee-c101397b2cd5
Source feed: FDA_Inspections

> FDA inspection 1008069 of CooperVision, Inc., April 13, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1008069
- Company Name: CooperVision, Inc.
- Inspection Date: 2017-04-13
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1169289 - 2022-05-04](https://www.keypedia.com/records/fda_inspections/coopervision-inc/84264b23-565f-4fc2-9d26-e9f10dd61e37)
- FDA Inspection 752767 - 2011-11-21
- [FDA Inspection 542489 - 2008-10-03](https://www.keypedia.com/records/fda_inspections/coopervision-inc/1963016b-df41-4cf3-9fda-87b6785dc944)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/elizabeth-h-slazak/1179c46f-556a-46f1-9114-66a6c809ce56)
- [Issuing Officer](https://www.keypedia.com/people/matthew-d-schnittker/cf76f07f-db6d-47a0-8412-7eb084d4fe8b)

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