# FDA Inspection 1067913 - Leghe Leggere Lavorate Srl - September 12, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/leghe-leggere-lavorate-srl/0be10868-50c1-441b-bd9d-f36e6f945e7a
Source feed: FDA_Inspections

> FDA Inspection 1067913 for Leghe Leggere Lavorate Srl on September 12, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1067913
- Company Name: Leghe Leggere Lavorate Srl
- Inspection Date: 2018-09-12
- 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/leghe-leggere-lavorate-srl/e6fd220e-e50d-4a37-b02a-4f180a29a46c

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