FDA Inspection 786547 — Acme-Monaco Corporation

Acme-Monaco Corporation — FEI 1000121071

The FDA completed an inspection of Acme-Monaco Corporation on May 17, 2012 in Presque Isle, ME. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 17, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Presque Isle, ME (United States)

Citations

IDCFRDescription
1472221 CFR 820.40Procedures not adequately established or maintained
232821 CFR 820.22Quality audits - auditor independence
368221 CFR 820.70(d)Implementing Personnel Procedures, Health, Cleanliness.