# Sintea Plustek LLC – FDA Inspection, Jul 30, 2024

Source: https://www.keypedia.com/records/fda_inspections/sintea-plustek-llc/d361eabe-e0ce-4c7a-84e8-3262906801a6
Source feed: FDA_Inspections

> FDA inspection 1245576 of Sintea Plustek LLC, July 30, 2024. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1245576
- Company Name: Sintea Plustek LLC
- Inspection Date: 2024-07-30
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1165821 - 2022-02-15

## Related Officers

- [Company Rep](https://www.keypedia.com/people/ronald-ifraimov/b4ce8b79-3fa2-4862-b7a4-68e14e45d87a)

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