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FDA Inspection
•Peregrine Surgical Ltd•February 7, 2013

Peregrine Surgical Ltd – FDA Inspection, Feb 7, 2013

Record Details

This FDA Inspection record concerns Peregrine Surgical Ltd, with an inspection on February 7, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company
Peregrine Surgical Ltd
Inspection Date
February 7, 2013
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · df846a99-8e55-498d-b951-94dd2e955718

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
817610
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Peregrine Surgical Ltd

5
DateClassificationOfficeProject area
September 26, 2018NAICenter for Devices and Radiological HealthRadiation Control and Health Safety Act
June 27, 2018Not classifiedPhiladelphia District Office
June 19, 2015VAICenter for Devices and Radiological HealthCompliance: Devices
June 30, 2011VAICenter for Devices and Radiological HealthCompliance: Devices
July 15, 2010OAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Peregrine Surgical Ltd
  • FDA Inspection 1069679 - 2018-09-26
  • FDA Inspection 1079992 - 2018-06-27
  • FDA Inspection 928467 - 2015-06-19
  • FDA Inspection 733958 - 2011-06-30
  • FDA Inspection 672519 - 2010-07-15

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