FDA Inspection 941155 — Merz North America, Inc.

Merz North America, Inc. — FEI 1012187

The FDA completed an inspection of Merz North America, Inc. on August 7, 2015 in Raleigh, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 7, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Raleigh, NC (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)