FDA Inspection 1013187 — Trewavis Surgical Instruments Pty Ltd.

Trewavis Surgical Instruments Pty Ltd. — FEI 3006795395

The FDA completed an inspection of Trewavis Surgical Instruments Pty Ltd. on Feb 7, 2017 in Bayswater. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 7, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Bayswater (Australia)