# FDA Inspection 820588 - Oculus Surgical, Inc. - March 01, 2013

Source: https://www.keypedia.com/records/fda_inspections/oculus-surgical-inc/2ebf40cd-131c-47a0-8ffb-cbe2e57c1aff
Source feed: FDA_Inspections

> FDA inspection 820588 of Oculus Surgical, Inc., March 01, 2013. Classification: Voluntary Action Indicated (VAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 820588
- Company Name: Oculus Surgical, Inc.
- Inspection Date: 2013-03-01
- 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: 0

## Related Documents

- FDA Inspection 1034626 - 2017-12-11
- [FDA Inspection 916800 - 2015-02-27](https://www.keypedia.com/records/fda_inspections/oculus-surgical-inc/f8eb3d0d-abd0-4ccb-85af-54e8ab575cc7)
- [FDA Inspection 768493 - 2012-02-17](https://www.keypedia.com/records/fda_inspections/oculus-surgical-inc/fad76235-47f6-48de-8ed7-1e6e99a35395)
- [FDA Inspection 660287 - 2010-05-03](https://www.keypedia.com/records/fda_inspections/oculus-surgical-inc/7fab8684-a46c-4e5d-b311-60b742be1069)

Company: https://www.keypedia.com/companies/oculus-surgical-inc/02bec6cc-18ae-46ce-b2a7-65c3e0d83472

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