FDA Inspection 798089 — ThyssenKrupp Access Manufacturing, LLC

ThyssenKrupp Access Manufacturing, LLC — FEI 1000139742

The FDA completed an inspection of ThyssenKrupp Access Manufacturing, LLC on September 6, 2012 in Roanoke, IL. 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 6, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Roanoke, IL (United States)