FDA inspection

Arthrosurface, Inc.: FDA inspection ending Oct 5, 2015

FDA inspection 947456 · Voluntary Action Indicated (VAI) · West Bridgewater, MA

Key facts

Inspection ID 947456
Firm Arthrosurface, Inc.
FEI number 3004154314
Address 28 Forge Pkwy
City West Bridgewater
State MA
ZIP 02379
Country United States
Fiscal year 2016
Inspection end date Oct 5, 2015
Classification Voluntary Action Indicated (VAI)
Project area Human Cellular, Tissue, and Gene Therapies
Product type Biologics

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
  • 1–9 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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