# CooperVision, Inc. - Inspection Records

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

> Inspection records and compliance data for CooperVision, Inc. in West Henrietta, New York. 4 FDA inspections on record (1 OAI), last inspected April 11, 2018.

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## Details

- Name: CooperVision, Inc.
- FEI Number: 3005724763
- Address Line 1: 180 Thruway Park Dr
- City: West Henrietta
- State: New York
- Zip Code: 14586
- Country Name: United States
- Address: 180 Thruway Park Dr, West Henrietta, New York 14586, United States
- Country: United States

## Related Documents

- FDA Inspection 1047905 - CooperVision, Inc. - 2018-04-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 11, 2018
- FDA Inspection 1047905 - CooperVision, Inc. - 2018-04-11 — classification: No Action Indicated (NAI), source: FDA, date: April 11, 2018
- FDA Inspection 783764 - CooperVision, Inc. - 2012-05-29 — classification: No Action Indicated (NAI), source: FDA, date: May 29, 2012
- FDA Inspection 783764 - CooperVision, Inc. - 2012-05-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 29, 2012
- [FDA Inspection 783764 - CooperVision, Inc. - 2012-05-29](https://www.keypedia.com/records/fda_inspections/coopervision-inc/95b42b13-2949-47dd-ba53-5bcc9fd28c6f) — classification: No Action Indicated (NAI), source: FDA, date: May 29, 2012
- FDA Inspection 751853 - CooperVision, Inc. - 2011-10-24 — classification: No Action Indicated (NAI), source: FDA, date: October 24, 2011
- [FDA Inspection 751853 - CooperVision, Inc. - 2011-10-24](https://www.keypedia.com/records/fda_inspections/coopervision-inc/87464afd-d545-497b-b12b-d658fc350cbc) — classification: Official Action Indicated (OAI), source: FDA, date: October 24, 2011
- FDA Inspection 598905 - CooperVision, Inc. - 2009-07-21 — classification: No Action Indicated (NAI), source: FDA, date: July 21, 2009
- FDA Inspection 598905 - CooperVision, Inc. - 2009-07-21 — classification: No Action Indicated (NAI), source: FDA, date: July 21, 2009

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