FDA Inspection 1130279 — BiOWiSH Technologies

BiOWiSH Technologies — FEI 3012697450

The FDA completed an inspection of BiOWiSH Technologies on September 2, 2020 in Blue Ash, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Veterinary.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 2, 2020
Fiscal Year
2020
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Blue Ash, OH (United States)