FDA inspection

Vericel Corporation: FDA inspection ending Mar 19, 2014

FDA inspection 870615 · Voluntary Action Indicated (VAI) · Cambridge, MA

Key facts

Inspection ID 870615
Firm Vericel Corporation
FEI number 3002836339
Address 64 Sidney St
City Cambridge
State MA
ZIP 02139
Country United States
Fiscal year 2014
Inspection end date Mar 19, 2014
Classification Voluntary Action Indicated (VAI)
Project area Human Cellular, Tissue, and Gene Therapies
Product type Biologics

At a glance

  • None 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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