FDA Inspection 733958 — Peregrine Surgical Ltd

Peregrine Surgical Ltd — FEI 1000121498

The FDA completed an inspection of Peregrine Surgical Ltd on June 30, 2011 in New Britain, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 30, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
New Britain, PA (United States)