FDA Inspection 1029517 — Alfa Wassermann, Inc.

Alfa Wassermann, Inc. — FEI 1000122044

The FDA completed an inspection of Alfa Wassermann, Inc. on August 23, 2017 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
August 23, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
West Caldwell, NJ (United States)