FDA Inspection 737266 — Gardner Denver Thomas Inc

Gardner Denver Thomas Inc — FEI 3007725233

The FDA completed an inspection of Gardner Denver Thomas Inc on Aug 3, 2011 in Monroe, LA. 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
Aug 3, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Monroe, LA (United States)