FDA Inspection 1279932 — Trident Manufacturing, Inc.
The FDA completed an inspection of Trident Manufacturing, Inc. on Aug 28, 2025 in Pingree Grove, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 3 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Aug 28, 2025
- Fiscal Year
- 2025
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Pingree Grove, IL (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 14713 | 21 CFR 820.198(a) | Lack of or inadequate complaint procedures |
| 2269 | 21 CFR 820.20(a) | Quality policy and objectives |
| 3282 | 21 CFR 820.90(a) | Nonconforming product, Lack of or inadequate procedures |