FDA Inspection 992629 — Alfa Wassermann, Inc.

Alfa Wassermann, Inc. — FEI 1000122044

The FDA completed an inspection of Alfa Wassermann, Inc. on October 28, 2016 in West Caldwell, NJ. 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
October 28, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
West Caldwell, NJ (United States)