FDA Inspection
Oculus Surgical, Inc.FDA Inspection 820588 - Oculus Surgical, Inc. - March 01, 2013
Record Details
This FDA Inspection record concerns Oculus Surgical, Inc., with an inspection on March 1, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Oculus Surgical, Inc.
- Inspection Date
- March 1, 2013
- Product Type
- Devices
View Company Profile
ID · 2ebf40cd-131c-47a0-8ffb-cbe2e57c1aff
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 820588
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Oculus Surgical, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| December 11, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 27, 2015 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 17, 2012 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 3, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Oculus Surgical, Inc.
- FDA Inspection 1034626 - 2017-12-11
- FDA Inspection 916800 - 2015-02-27
- FDA Inspection 768493 - 2012-02-17
- FDA Inspection 660287 - 2010-05-03
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