FDA Inspection 1064722 — Litex Manufacturing, Inc
The FDA completed an inspection of Litex Manufacturing, Inc on August 13, 2018 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 13, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Glendale, CA (United States)