# FDA Inspection 716018 - Optovue, Inc. - April 07, 2011

Source: https://www.keypedia.com/records/fda_inspections/optovue-inc/0e510e3f-5865-4ff4-b43c-9b9bb0db086f
Source feed: FDA_Inspections

> FDA Inspection 716018 for Optovue, Inc. on April 07, 2011. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 716018
- Company Name: Optovue, Inc.
- Inspection Date: 2011-04-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1006623 - 2017-03-20](https://www.keypedia.com/records/fda_inspections/optovue-inc/98344128-6aec-4ead-a82c-453d2e3e3fbd)
- [FDA Inspection 1006623 - 2017-03-20](https://www.keypedia.com/records/fda_inspections/optovue-inc/f830a4fe-d94e-4e56-b218-218e6e45d5dc)
- [FDA Inspection 982436 - 2016-04-14](https://www.keypedia.com/records/fda_inspections/optovue-inc/0e0cf597-3e48-4eb9-86d9-437e8e859b8e)
- [FDA Inspection 855282 - 2013-11-15](https://www.keypedia.com/records/fda_inspections/optovue-inc/b3f2955b-faba-48b7-b99f-e4f5d51d973b)
- [FDA Inspection 795211 - 2012-09-14](https://www.keypedia.com/records/fda_inspections/optovue-inc/cf66ba8f-ec8b-43b1-9eec-b548e51ca07a)

Company: https://www.keypedia.com/companies/optovue-inc/4bd8cfe7-d0f3-4543-87c1-b45a72a966b8

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