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FDA Inspection 572524 — Memtec Incorporated

Memtec Incorporated — FEI 3001617772

The FDA completed an inspection of Memtec Incorporated on March 26, 2009 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
March 26, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Salem, NH (United States)

Facility

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FDA data resources