# Optovue, Inc. – FDA Inspection, Nov 15, 2013

Source: https://www.keypedia.com/records/fda_inspections/optovue-inc/b3f2955b-faba-48b7-b99f-e4f5d51d973b
Source feed: FDA_Inspections

> FDA inspection 855282 of Optovue, Inc., November 15, 2013. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 855282
- Company Name: Optovue, Inc.
- Inspection Date: 2013-11-15
- 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: 3

## Related Documents

- [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
- [FDA Inspection 795211 - 2012-09-14](https://www.keypedia.com/records/fda_inspections/optovue-inc/cf66ba8f-ec8b-43b1-9eec-b548e51ca07a)
- FDA Inspection 716018 - 2011-04-07
- [FDA Inspection 639717 - 2010-01-08](https://www.keypedia.com/records/fda_inspections/optovue-inc/9184a242-4dba-4ab0-9c18-a2f3340bcee8)

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