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FDA Inspection 1001311 — Porex Corporation

Porex Corporation — FEI 1043678

The FDA completed an inspection of Porex Corporation on February 2, 2017 in Fairburn, GA. 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 2, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Fairburn, GA (United States)

Facility

Other inspections at this facility

  • 1123271 (NAI Wed Mar 11 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 828983 (NAI Thu Apr 25 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 809891 (NAI Wed Nov 28 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 614728 (NAI Thu Sep 24 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources