FDA Inspection 1125740 — Antech Diagnostics GLP
The FDA completed an inspection of Antech Diagnostics GLP on July 16, 2020 in Morrisville, NC. 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
- July 16, 2020
- Fiscal Year
- 2020
- Product Type
- Veterinary
- Project Area
- Monitoring of Marketed Animal Drugs, Feed, and Devices
- Location
- Morrisville, NC (United States)