FDA Inspection 817610 — Peregrine Surgical Ltd

Peregrine Surgical Ltd — FEI 1000121498

The FDA completed an inspection of Peregrine Surgical Ltd on February 7, 2013 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 7, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
New Britain, PA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures