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FDA Inspection
•General Physiotherapy Inc•August 23, 2018

General Physiotherapy Inc – FDA Inspection, Aug 23, 2018

Record Details

This FDA Inspection record concerns General Physiotherapy Inc, with an inspection on August 23, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company
General Physiotherapy Inc
Inspection Date
August 23, 2018
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Edward E. Lockwood (Issuing Officer)
View Company Profile

ID · 995bed0f-5d96-432d-b142-a5e03df7d569

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1063738
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

Other FDA inspections of General Physiotherapy Inc

5
DateClassificationOfficeProject area
March 12, 2025NAIKansas City District OfficePostmarket Assurance: Medical Devices
July 1, 2022VAICenter for Devices and Radiological HealthCompliance: Devices
November 7, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
August 16, 2012VAICenter for Devices and Radiological HealthCompliance: Devices
February 22, 2010VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for General Physiotherapy Inc
  • FDA Inspection 1263549 - 2025-03-12
  • FDA Inspection 1173677 - 2022-07-01
  • FDA Inspection 854640 - 2013-11-07
  • FDA Inspection 796608 - 2012-08-16
  • FDA Inspection 647781 - 2010-02-22

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