FDA Inspection 896887 — Merz North America, Inc.

Merz North America, Inc. — FEI 1012187

The FDA completed an inspection of Merz North America, Inc. on August 15, 2014 in Raleigh, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 15, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Raleigh, NC (United States)

Citations

IDCFRDescription
337521 CFR 820.198(e)Records of complaint investigation