FDA Inspection 1100117 — NEOTERYX, LLC
The FDA completed an inspection of NEOTERYX, LLC on August 15, 2019 in Torrance, CA. 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 15, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Torrance, CA (United States)