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FDA Inspection
•Trewavis Surgical Instruments Pty Ltd.•February 7, 2017

Trewavis Surgical Instruments Pty Ltd. – FDA Inspection, Feb 7, 2017

Record Details

This FDA Inspection record concerns Trewavis Surgical Instruments Pty Ltd., with an inspection on February 7, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Trewavis Surgical Instruments Pty Ltd.
Inspection Date
February 7, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Shaquenta Y. Perkins (Issuing Officer)
View Company Profile

ID · 3d970695-b2f6-440c-90ca-0218eff6b978

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1013187
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

Other FDA inspections of Trewavis Surgical Instruments Pty Ltd.

2
DateClassificationOfficeProject area
January 22, 2025NAICenter for Devices and Radiological HealthCompliance: Devices
August 17, 2022VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Trewavis Surgical Instruments Pty Ltd.
  • FDA Inspection 1260936 - 2025-01-22
  • FDA Inspection 1177941 - 2022-08-17

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