FDA Inspection 1062131 — PATHWAY MEDTECH, LLC
The FDA completed an inspection of PATHWAY MEDTECH, LLC on Aug 3, 2018 in Santee, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Aug 3, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Santee, CA (United States)