FDA inspection

Perma Pure LLC: FDA inspection ending Mar 18, 2011

FDA inspection 713530 · Official Action Indicated (OAI) · Lakewood, NJ

Key facts

Inspection ID 713530
Firm Perma Pure LLC
FEI number 2244684
Address 1001 New Hampshire Ave Unit B
City Lakewood
State NJ
ZIP 08701
Country United States
Fiscal year 2011
Inspection end date Mar 18, 2011
Classification Official Action Indicated (OAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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