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FDA Inspection 683171 — Repro-Med Systems, Inc.

Repro-Med Systems, Inc. — FEI 1318360

The FDA completed an inspection of Repro-Med Systems, Inc. on September 21, 2010 in Chester, NY. 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
September 21, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Chester, NY (United States)

Facility

Other inspections at this facility

  • 1029627 (VAI Thu Oct 19 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 996093 (VAI Fri Dec 16 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 929452 (OAI Tue Jun 23 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 793650 (NAI Fri Jul 20 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 627589 (NAI Wed Oct 28 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources