FDA Inspection 1294056 — Jedmed Instrument Company
The FDA completed an inspection of Jedmed Instrument Company on December 5, 2025 in Saint Louis, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 4 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- December 5, 2025
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Saint Louis, MO (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 2350 | 21 CFR 820.25(b) | Training - Lack of or inadequate procedures |
| 3149 | 21 CFR 820.180 | Availability |
| 3168 | 21 CFR 820.198(a) | Complaints |
| 3206 | 21 CFR 820.50(b) | Approval, inadequate purchasing data |