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FDA Inspection
•Hoya Corporation - Pentax Life Division•September 7, 2018

Hoya Corporation - Pentax Life Division – FDA Inspection, Sep 7, 2018

Record Details

This FDA Inspection record concerns Hoya Corporation - Pentax Life Division, with an inspection on September 7, 2018, issued by the Office of Inspections and Investigations, covering medical devices & rad health.

Company
Hoya Corporation - Pentax Life Division
Inspection Date
September 7, 2018
Product Type
Medical Devices & Rad Health
Office
Office of Inspections and Investigations
View Company Profile

ID · c312148d-6a19-4d07-9ec3-6141ea20ecc5

Inspection Facts

Inspection number
1131698
FDA center
Medical Devices & Rad Health
Outcome
Form 483 issued

Other FDA inspections of Hoya Corporation - Pentax Life Division

3
DateClassificationOfficeProject area
August 10, 2023Not classifiedOffice of Inspections and Investigations
April 21, 2015OAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
July 15, 2014NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Hoya Corporation - Pentax Life Division
  • FDA Inspection 1215013 - 2023-08-10
  • FDA Inspection 925512 - 2015-04-21
  • FDA Inspection 890110 - 2014-07-15

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