FDA Inspection
Oculus Surgical, Inc.FDA Inspection 1034626 - Oculus Surgical, Inc. - December 11, 2017
Record Details
This FDA Inspection record concerns Oculus Surgical, Inc., with an inspection on December 11, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Oculus Surgical, Inc.
- Inspection Date
- December 11, 2017
- Product Type
- Devices
View Company Profile
ID · 19ae0bd6-f0ec-418a-b224-81122b9ddc27
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1034626
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Oculus Surgical, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| February 27, 2015 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 1, 2013 | NAI | 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.
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