FDA Inspection 1244590 — KDI Med Supply
The FDA completed an inspection of KDI Med Supply on Jul 15, 2024 in Fremont, OH. 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
- Jul 15, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Fremont, OH (United States)