FDA Inspection 1148524 — Litex Manufacturing, Inc
The FDA completed an inspection of Litex Manufacturing, Inc on August 5, 2021 in Glendale, 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 5, 2021
- Fiscal Year
- 2021
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Glendale, CA (United States)