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FDA Inspection
•Optovue, Inc.•March 20, 2017

Optovue, Inc. – FDA Inspection, Mar 20, 2017

Record Details

This FDA Inspection record concerns Optovue, Inc., with an inspection on March 20, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Optovue, Inc.
Inspection Date
March 20, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Jude C. Dike (Investigator)
View Company Profile

ID · f830a4fe-d94e-4e56-b218-218e6e45d5dc

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1006623
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of Optovue, Inc.

5
DateClassificationOfficeProject area
April 14, 2016NAICenter for Devices and Radiological HealthCompliance: Devices
November 15, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
September 14, 2012OAICenter for Devices and Radiological HealthCompliance: Devices
April 7, 2011NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
January 8, 2010OAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Optovue, Inc.
  • FDA Inspection 982436 - 2016-04-14
  • FDA Inspection 855282 - 2013-11-15
  • FDA Inspection 795211 - 2012-09-14
  • FDA Inspection 716018 - 2011-04-07
  • FDA Inspection 639717 - 2010-01-08

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