# FDA Inspection 1165821 - Sintea Plustek LLC - February 15, 2022

Source: https://www.keypedia.com/records/fda_inspections/sintea-plustek-llc/10b2906a-7ba5-4f75-a668-26a2a7fce640
Source feed: FDA_Inspections

> FDA Inspection 1165821 for Sintea Plustek LLC on February 15, 2022. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1165821
- Company Name: Sintea Plustek LLC
- Inspection Date: 2022-02-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1245576 - 2024-07-30](https://www.keypedia.com/records/fda_inspections/sintea-plustek-llc/1b65839c-1a21-4e14-9bde-f0e7d25fc0ff)
- [FDA Inspection 1245576 - 2024-07-30](https://www.keypedia.com/records/fda_inspections/sintea-plustek-llc/d361eabe-e0ce-4c7a-84e8-3262906801a6)
- [FDA Inspection 1165821 - 2022-02-15](https://www.keypedia.com/records/fda_inspections/sintea-plustek-llc/0e5c8d59-c95b-4d56-9fa1-d73f9f1f1449)

Company: https://www.keypedia.com/companies/sintea-plustek-llc/6d336bbd-fd28-42ab-82a8-e384cc7a55fb

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7