FDA Inspection 797414 — Philips Ultrasound, Inc

Philips Ultrasound, Inc — FEI 2518586

The FDA completed an inspection of Philips Ultrasound, Inc on Sep 5, 2012 in Reedsville, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 5, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Reedsville, PA (United States)

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