FDA inspection

Life Recovery Systems HD, LLC: FDA inspection ending Aug 14, 2012

FDA inspection 794489 · No Action Indicated (NAI) · Kinnelon, NJ

Key facts

Inspection ID 794489
Firm Life Recovery Systems HD, LLC
FEI number 3006059109
Address 170 Kinnelon Rd Ste 8
City Kinnelon
State NJ
ZIP 07405
Country United States
Fiscal year 2012
Inspection end date Aug 14, 2012
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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