FDA inspection

Osteotech, Inc.: FDA inspection ending Dec 7, 2006

FDA inspection 455906 · No Action Indicated (NAI) · Eatontown, NJ

Key facts

Inspection ID 455906
Firm Osteotech, Inc.
FEI number 3002600221
Address 201 Industrial Way W
City Eatontown
State NJ
ZIP 07724-2205
Fiscal year 2007
Inspection end date Dec 7, 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
  • 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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