FDA Inspection 854123 — Memtec Incorporated

Memtec Incorporated — FEI 3001617772

The FDA completed an inspection of Memtec Incorporated on November 6, 2013 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 6, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Salem, NH (United States)