FEI establishment

Vericel Corporation

FDA establishment FEI 3002836339 · Cambridge, United States

Key facts

FEI number 3002836339
Legal name Vericel Corporation
City Cambridge
Country United States
Product types Biologics, Devices, Drugs
Drug operations ANALYSIS, API MANUFACTURE, LABEL, MANUFACTURE, PACK
Last inspection Jun 12, 2026

At a glance

  • 10–99 FDA inspections
  • 1–9 No Action Indicated (NAI)
  • 10–99 Voluntary Action Indicated (VAI)
  • None Official Action Indicated (OAI)
  • 10–99 Inspections with a Form 483
  • 10–99 Citations
  • 1–9 Repeat citations
  • None Warning letters
  • None Linked 510(k)s

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA establishments (FEI)

An FEI (FDA Establishment Identifier) is the number the FDA assigns to a site it inspects. FEIs of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection and compliance data

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