FDA Inspection 1120592 — InterX Technologies
The FDA completed an inspection of InterX Technologies on February 13, 2020 in Plano, TX. 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
- February 13, 2020
- Fiscal Year
- 2020
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Plano, TX (United States)