# FDA Inspection 650559 - Sintea Plustek S.p.A. - February 04, 2010

Source: https://www.globalkeysolutions.net/records/fda_inspections/sintea-plustek-spa/0d8aec80-c6fd-4a93-a83a-6665b30ca073
Source feed: FDA_Inspections

> FDA Inspection 650559 for Sintea Plustek S.p.A. on February 04, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 650559
- Company Name: Sintea Plustek S.p.A.
- Inspection Date: 2010-02-04
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1063008 - 2018-07-19](https://www.globalkeysolutions.net/records/fda_inspections/sintea-plustek-spa/a0af4e64-b65f-46b9-8ebc-4bee3c10711b)

Company: https://www.globalkeysolutions.net/companies/sintea-plustek-spa/a9273a69-aae9-4274-a61d-927942f1f6ba

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