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FDA Inspection
•Hoya Corporation - Pentax Life Division•July 15, 2014

Hoya Corporation - Pentax Life Division – FDA Inspection, Jul 15, 2014

Record Details

This FDA Inspection record concerns Hoya Corporation - Pentax Life Division, with an inspection on July 15, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company
Hoya Corporation - Pentax Life Division
Inspection Date
July 15, 2014
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · a21538d2-f4ee-46da-8515-518639b3685b

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
890110
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Hoya Corporation - Pentax Life Division

3
DateClassificationOfficeProject area
August 10, 2023Not classifiedOffice of Inspections and Investigations
September 7, 2018Not classifiedOffice of Inspections and Investigations
April 21, 2015OAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Hoya Corporation - Pentax Life Division
  • FDA Inspection 1215013 - 2023-08-10
  • FDA Inspection 1131698 - 2018-09-07
  • FDA Inspection 925512 - 2015-04-21

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