FDA Inspection 660475 — Ametek, Inc.

Ametek, Inc. — FEI 1000111097

The FDA completed an inspection of Ametek, Inc. on April 30, 2010 in Largo, FL. 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
April 30, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Largo, FL (United States)