FDA Inspection 1304160 — Myrava Inc
The FDA completed an inspection of Myrava Inc on Feb 10, 2026 in Parma, 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
- Feb 10, 2026
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Parma, OH (United States)