FDA Inspection 982018 — Acme Monaco Corporation

Acme Monaco Corporation — FEI 1293141

The FDA completed an inspection of Acme Monaco Corporation on August 24, 2016 in New Britain, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 24, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
New Britain, CT (United States)