FDA Inspection 1067913 — Leghe Leggere Lavorate Srl

Leghe Leggere Lavorate Srl — FEI 3005059805

The FDA completed an inspection of Leghe Leggere Lavorate Srl on Sep 12, 2018 in Buccinasco. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 12, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Buccinasco (Italy)