FDA inspection

Vericel Corporation: FDA inspection ending Sep 19, 2008

FDA inspection 537019 · Voluntary Action Indicated (VAI) · Cambridge, MA

Key facts

Inspection ID 537019
Firm Vericel Corporation
FEI number 3002836339
Address 64 Sidney St
City Cambridge
State MA
ZIP 02139-4170
Fiscal year 2008
Inspection end date Sep 19, 2008
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • 1–9 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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