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FDA Inspection 1115239 — Perma Pure LLC

Perma Pure LLC — FEI 2244684

The FDA completed an inspection of Perma Pure LLC on January 3, 2020 in Lakewood, NJ. 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
January 3, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Lakewood, NJ (United States)

Facility

Other inspections at this facility

  • 1309030 (NAI Fri Mar 06 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 956470 (NAI Thu Jan 21 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 838041 (NAI Tue Jul 09 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 745531 (VAI Mon Sep 19 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 713530 (OAI Fri Mar 18 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources