# FDA Inspection 1087874 - Keter Italia S.P.A. - February 07, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/keter-italia-spa/a8cb69c4-cc3c-4cc1-ae7e-c849b6184342
Source feed: FDA_Inspections

> FDA Inspection 1087874 for Keter Italia S.P.A. on February 07, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1087874
- Company Name: Keter Italia S.P.A.
- Inspection Date: 2019-02-07
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/keter-italia-spa/ef3e3f05-4e46-45da-b8e0-0706234da946

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