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FDA Inspection
•Oculus Surgical, Inc.•December 11, 2017

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
Office
Center for Devices and Radiological Health
View Company Profile

ID · 5ffa6351-a345-48ca-a215-27b265e7176d

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1034626
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of Oculus Surgical, Inc.

4
DateClassificationOfficeProject area
February 27, 2015VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
March 1, 2013NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
February 17, 2012OAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
May 3, 2010VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Oculus Surgical, Inc.
  • FDA Inspection 916800 - 2015-02-27
  • FDA Inspection 820588 - 2013-03-01
  • FDA Inspection 768493 - 2012-02-17
  • FDA Inspection 660287 - 2010-05-03

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