FDA inspection

Nephros, Inc.: FDA inspection ending Jun 1, 2006

FDA inspection 430869 · No Action Indicated (NAI) · South Orange, NJ

Key facts

Inspection ID 430869
Firm Nephros, Inc.
FEI number 3003337893
Address 380 Lackawanna Pl
City South Orange
State NJ
ZIP 07079-1704
Fiscal year 2006
Inspection end date Jun 1, 2006
Classification No Action Indicated (NAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 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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