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FDA Inspection
•PHC Corporation•December 25, 2017

PHC Corporation – FDA Inspection, Dec 25, 2017

Record Details

This FDA Inspection record concerns PHC Corporation, with an inspection on December 25, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
PHC Corporation
Inspection Date
December 25, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Sean T. Creighton
View Company Profile

ID · a27bdb17-fac9-42ef-9c6b-bee80646d315

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1040858
FDA center
Medical Devices & Rad Health
Project area
Bioresearch Monitoring
Outcome
Form 483 issued

Other FDA inspections of PHC Corporation

3
DateClassificationOfficeProject area
February 2, 2023NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
February 4, 2014NAICenter for Devices and Radiological HealthCompliance: Devices
April 9, 2009NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for PHC Corporation
  • FDA Inspection 1196545 - 2023-02-02
  • FDA Inspection 867176 - 2014-02-04
  • FDA Inspection 586599 - 2009-04-09

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