FDA inspection

Organogenesis, Inc.: FDA inspection ending May 26, 2017

FDA inspection 1014830 · No Action Indicated (NAI) · Canton, MA

Key facts

Inspection ID 1014830
Firm Organogenesis, Inc.
FEI number 1000148471
Address 10933 N Torrey Pines Rd
City Canton
State MA
ZIP 02021
Country United States
Fiscal year 2017
Inspection end date May 26, 2017
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
  • 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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