FDA Inspection 797414 — Philips Ultrasound, Inc

Philips Ultrasound, Inc — FEI 2518586

The FDA completed an inspection of Philips Ultrasound, Inc on September 5, 2012 in Reedsville, 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
September 5, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Reedsville, PA (United States)