FDA Inspection 1106102 — Archpoint Group

Archpoint Group — FEI 3011204629

The FDA completed an inspection of Archpoint Group on September 17, 2019 in San Antonio, TX. 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
September 17, 2019
Fiscal Year
2019
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
San Antonio, TX (United States)

Additional Details

FSVP