# Optovue, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/optovue-inc/4bd8cfe7-d0f3-4543-87c1-b45a72a966b8

> Inspection records and compliance data for Optovue, Inc. in Fremont, California. Access full analysis and detailed observations.

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## Details

- Name: Optovue, Inc.
- FEI Number: 3005950902
- City: Fremont
- State: California
- Country Name: United States
- Address Line 1: 2800 Bayview Dr
- Zip Code: 94538

## Related Documents

- [FDA Inspection 1006623 - Optovue, Inc. - 2017-03-20](https://www.globalkeysolutions.net/records/fda_inspections/optovue-inc/98344128-6aec-4ead-a82c-453d2e3e3fbd) — classification: No Action Indicated (NAI), source: FDA, date: March 20, 2017
- [FDA Inspection 1006623 - Optovue, Inc. - 2017-03-20](https://www.globalkeysolutions.net/records/fda_inspections/optovue-inc/f830a4fe-d94e-4e56-b218-218e6e45d5dc) — classification: No Action Indicated (NAI), source: FDA, date: March 20, 2017
- [FDA Inspection 982436 - Optovue, Inc. - 2016-04-14](https://www.globalkeysolutions.net/records/fda_inspections/optovue-inc/0e0cf597-3e48-4eb9-86d9-437e8e859b8e) — classification: No Action Indicated (NAI), source: FDA, date: April 14, 2016
- [FDA Inspection 855282 - Optovue, Inc. - 2013-11-15](https://www.globalkeysolutions.net/records/fda_inspections/optovue-inc/b3f2955b-faba-48b7-b99f-e4f5d51d973b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 15, 2013
- [FDA Inspection 795211 - Optovue, Inc. - 2012-09-14](https://www.globalkeysolutions.net/records/fda_inspections/optovue-inc/038690bd-1986-4c20-b243-9c3bac351f02) — classification: No Action Indicated (NAI), source: FDA, date: September 14, 2012
- [FDA Inspection 795211 - Optovue, Inc. - 2012-09-14](https://www.globalkeysolutions.net/records/fda_inspections/optovue-inc/cf66ba8f-ec8b-43b1-9eec-b548e51ca07a) — classification: Official Action Indicated (OAI), source: FDA, date: September 14, 2012
- [FDA Inspection 716018 - Optovue, Inc. - 2011-04-07](https://www.globalkeysolutions.net/records/fda_inspections/optovue-inc/0e510e3f-5865-4ff4-b43c-9b9bb0db086f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 7, 2011
- [FDA Inspection 716018 - Optovue, Inc. - 2011-04-07](https://www.globalkeysolutions.net/records/fda_inspections/optovue-inc/842b2831-487f-41f5-a926-49ea54c18848) — classification: No Action Indicated (NAI), source: FDA, date: April 7, 2011
- [FDA Inspection 639717 - Optovue, Inc. - 2010-01-08](https://www.globalkeysolutions.net/records/fda_inspections/optovue-inc/3dc0d7b1-5bd5-481e-8dc1-0659d03ee51c) — classification: Official Action Indicated (OAI), source: FDA, date: January 8, 2010
- [FDA Inspection 639717 - Optovue, Inc. - 2010-01-08](https://www.globalkeysolutions.net/records/fda_inspections/optovue-inc/9184a242-4dba-4ab0-9c18-a2f3340bcee8) — classification: Official Action Indicated (OAI), source: FDA, date: January 8, 2010

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