FDA Inspection 982018 — Acme Monaco Corporation

Acme Monaco Corporation — FEI 1293141

The FDA completed an inspection of Acme Monaco Corporation on Aug 24, 2016 in New Britain, CT. 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
Aug 24, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
New Britain, CT (United States)

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