FDA Inspection 1247721 — Anthrotronix, Inc.
The FDA completed an inspection of Anthrotronix, Inc. on August 14, 2024 in Silver Spring, MD. 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 14, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Silver Spring, MD (United States)