# FDA Inspection 1047905 - CooperVision, Inc. - April 11, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/coopervision-inc/dcd1f1c9-5a5e-4b65-bf19-12f016b1e0e5
Source feed: FDA_Inspections

> FDA Inspection 1047905 for CooperVision, Inc. on April 11, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1047905
- Company Name: CooperVision, Inc.
- Inspection Date: 2018-04-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1047905 - 2018-04-11](https://www.globalkeysolutions.net/records/fda_inspections/coopervision-inc/8d97f656-ca8c-441e-ab8b-7a240f7c5176)
- [FDA Inspection 783764 - 2012-05-29](https://www.globalkeysolutions.net/records/fda_inspections/coopervision-inc/95b42b13-2949-47dd-ba53-5bcc9fd28c6f)
- [FDA Inspection 783764 - 2012-05-29](https://www.globalkeysolutions.net/records/fda_inspections/coopervision-inc/6b49db1a-dafb-4819-b739-457943d5d1b6)
- [FDA Inspection 783764 - 2012-05-29](https://www.globalkeysolutions.net/records/fda_inspections/coopervision-inc/37bc7772-a52d-46f1-bc64-bc4ca7f2c326)
- [FDA Inspection 751853 - 2011-10-24](https://www.globalkeysolutions.net/records/fda_inspections/coopervision-inc/87464afd-d545-497b-b12b-d658fc350cbc)

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

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