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FDA Inspection 858023 — AMCO International Manufacturing & Design, Inc.

AMCO International Manufacturing & Design, Inc. — FEI 3005906887

The FDA completed an inspection of AMCO International Manufacturing & Design, Inc. on November 21, 2013 in Brooklyn, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 21, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Brooklyn, NY (United States)

Facility

Other inspections at this facility

  • 1234377 (OAI Wed Mar 20 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1142703 (VAI Thu May 27 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1081946 (NAI Tue Jun 26 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 933091 (VAI Tue Jun 30 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 775103 (VAI Wed Mar 28 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources