FDA Inspection 1023115 — Rockport Hutterian Brethren, Inc.

Rockport Hutterian Brethren, Inc. — FEI 1717282

The FDA completed an inspection of Rockport Hutterian Brethren, Inc. on August 22, 2017 in Alexandria, SD. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 22, 2017
Fiscal Year
2017
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Alexandria, SD (United States)