FDA inspection

Arthrosurface, Inc.: FDA inspection ending Aug 6, 2025

FDA inspection 1279142 · No Action Indicated (NAI) · West Bridgewater, MA

Key facts

Inspection ID 1279142
Firm Arthrosurface, Inc.
FEI number 3004154314
Address 319 Manley St
City West Bridgewater
State MA
ZIP 02379
Country United States
Fiscal year 2025
Inspection end date Aug 6, 2025
Classification No Action Indicated (NAI)
Project area Human Cellular, Tissue, and Gene Therapies
Product type Biologics

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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