FDA Inspection 1025795 — Aros Surgical Instruments Corporation

Aros Surgical Instruments Corporation — FEI 1000135614

The FDA completed an inspection of Aros Surgical Instruments Corporation on August 29, 2017 in North Wales, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 29, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
North Wales, PA (United States)