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FDA Inspection 949589 — Memtec Incorporated

Memtec Incorporated — FEI 3001617772

The FDA completed an inspection of Memtec Incorporated on November 20, 2015 in Salem, NH. 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
November 20, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Salem, NH (United States)

Facility

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  • 854123 (NAI Wed Nov 06 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 752409 (NAI Mon Oct 31 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 572524 (NAI Thu Mar 26 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources