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FDA Inspection 1003651 — Kem Medical Products Corp

Kem Medical Products Corp — FEI 2432141

The FDA completed an inspection of Kem Medical Products Corp on February 21, 2017 in Hauppauge, 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
February 21, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Hauppauge, NY (United States)

Facility

Other inspections at this facility

  • 1175436 (VAI Thu Jul 21 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1115221 (VAI Wed Jan 15 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 791042 (NAI Tue Jul 10 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 623870 (VAI Tue Oct 27 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources