FDA Inspection 1298384 — OKAPI MEDICAL
The FDA completed an inspection of OKAPI MEDICAL on December 4, 2025 in Akron, OH. 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
- December 4, 2025
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Akron, OH (United States)