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FDA Inspection 1209243 — Merz North America, Inc.

Merz North America, Inc. — FEI 1012187

The FDA completed an inspection of Merz North America, Inc. on June 22, 2023 in Raleigh, NC. 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
June 22, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Raleigh, NC (United States)

Additional Details

Sponsor, Contract Research Organization

Facility

Other inspections at this facility

  • 1290810 (NAI Tue Oct 28 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1103289 (NAI Wed Sep 18 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1060604 (VAI Thu Jul 26 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 941155 (NAI Fri Aug 07 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 912381 (NAI Mon Jan 26 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources