FDA Inspection 920763 — Merz North America

Merz North America — FEI 3011234890

The FDA completed an inspection of Merz North America on Mar 31, 2015 in San Mateo, CA. 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
Mar 31, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
San Mateo, CA (United States)

Additional details

Sponsor, Contract Research Organization

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