FDA Inspection 1245576 — Sintea Plustek LLC
The FDA completed an inspection of Sintea Plustek LLC on Jul 30, 2024 in Miami Beach, FL. 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
- Jul 30, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Miami Beach, FL (United States)