FDA Inspection 1290810 — Merz North America, Inc.

Merz North America, Inc. — FEI 1012187

The FDA completed an inspection of Merz North America, Inc. on Oct 28, 2025 in Raleigh, NC. 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
Oct 28, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Raleigh, NC (United States)

Additional details

Sponsor, Contract Research Organization

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