FDA Inspection 834443 — Merz North America, Inc.

Merz North America, Inc. — FEI 3003407669

The FDA completed an inspection of Merz North America, Inc. on April 19, 2013 in Franksville, WI. 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 19, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Franksville, WI (United States)

Additional Details

Postmarket Audit Inspections