# FDA Inspection 1006623 - Optovue, Inc. - March 20, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/optovue-inc/f830a4fe-d94e-4e56-b218-218e6e45d5dc/
Source feed: FDA_Inspections

> FDA Inspection 1006623 for Optovue, Inc. on March 20, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1006623
- Company Name: Optovue, Inc.
- Inspection Date: 2017-03-20
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1006623 - 2017-03-20](https://www.globalkeysolutions.net/api/records/fda_inspections/optovue-inc/98344128-6aec-4ead-a82c-453d2e3e3fbd/)
- [FDA Inspection 982436 - 2016-04-14](https://www.globalkeysolutions.net/api/records/fda_inspections/optovue-inc/0e0cf597-3e48-4eb9-86d9-437e8e859b8e/)
- [FDA Inspection 855282 - 2013-11-15](https://www.globalkeysolutions.net/api/records/fda_inspections/optovue-inc/b3f2955b-faba-48b7-b99f-e4f5d51d973b/)
- [FDA Inspection 795211 - 2012-09-14](https://www.globalkeysolutions.net/api/records/fda_inspections/optovue-inc/cf66ba8f-ec8b-43b1-9eec-b548e51ca07a/)
- [FDA Inspection 795211 - 2012-09-14](https://www.globalkeysolutions.net/api/records/fda_inspections/optovue-inc/038690bd-1986-4c20-b243-9c3bac351f02/)

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

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