# FDA Inspection 916800 - Oculus Surgical, Inc. - February 27, 2015

Source: https://www.keypedia.com/records/fda_inspections/oculus-surgical-inc/d9c0e390-a740-4a7f-8b5d-c223e0072500
Source feed: FDA_Inspections

> FDA inspection 916800 of Oculus Surgical, Inc., February 27, 2015. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 916800
- Company Name: Oculus Surgical, Inc.
- Inspection Date: 2015-02-27
- 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: 4

## Related Documents

- FDA Inspection 1034626 - 2017-12-11
- [FDA Inspection 820588 - 2013-03-01](https://www.keypedia.com/records/fda_inspections/oculus-surgical-inc/abd30594-1c9d-4348-93d5-9ccbdf146bf1)
- [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