FDA Inspection 1079837 — Sanofi US Services Inc.

Sanofi US Services Inc. — FEI 3010770778

The FDA completed an inspection of Sanofi US Services Inc. on Feb 7, 2019 in Morristown, NJ. 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
Feb 7, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Morristown, NJ (United States)