FDA Inspection 1297220 — Assembly-Tek, LLC
The FDA completed an inspection of Assembly-Tek, LLC on December 17, 2025 in Dayton, 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 17, 2025
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Dayton, OH (United States)