FDA Inspection 1226927 — Merz North America, Inc.

Merz North America, Inc. — FEI 3013840437

The FDA completed an inspection of Merz North America, Inc. on Jan 3, 2024 in Sturtevant, WI. 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
Jan 3, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Sturtevant, WI (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.