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FDA Inspection
•Physio-Control, Inc.•March 29, 2019

Physio-Control, Inc. – FDA Inspection, Mar 29, 2019

Record Details

This FDA Inspection record concerns Physio-Control, Inc., with an inspection on March 29, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company
Physio-Control, Inc.
Inspection Date
March 29, 2019
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Paul M. Kawamoto (Company Rep)
View Company Profile

ID · fcc92493-f605-4615-b593-8ee0f4442d7c

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1086723
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of Physio-Control, Inc.

12
DateClassificationOfficeProject area
April 18, 2024NAICenter for Devices and Radiological HealthCompliance: Devices
November 26, 2019VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
December 15, 2017VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
November 18, 2016VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
June 26, 2015OAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
View all 12 other inspections on the company page
Other documents for Physio-Control, Inc.
  • FDA Inspection 1230558 - 2024-04-18
  • FDA Inspection 1111211 - 2019-11-26
  • FDA Inspection 1035043 - 2017-12-15
  • FDA Inspection 994067 - 2016-11-18
  • FDA Inspection 931792 - 2015-06-26

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