FDA Inspection 1165821 — Sintea Plustek LLC
The FDA completed an inspection of Sintea Plustek LLC on Feb 15, 2022 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
- Feb 15, 2022
- Fiscal Year
- 2022
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Miami Beach, FL (United States)