FDA Inspection 903178 — Acme Monaco Corporation

Acme Monaco Corporation — FEI 1293141

The FDA completed an inspection of Acme Monaco Corporation on Nov 5, 2014 in New Britain, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 5, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
New Britain, CT (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures

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