FDA Inspection 1077908 — LaVezzi Precision, A MW Industries Company

LaVezzi Precision, A MW Industries Company — FEI 1000220336

The FDA completed an inspection of LaVezzi Precision, A MW Industries Company on Nov 27, 2018 in Bloomingdale, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 27, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Bloomingdale, IL (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.