FDA inspection

ARTAFLEX BUFFALO INC: FDA inspection ending Jul 9, 2026

FDA inspection 1326396 · Voluntary Action Indicated (VAI) · Buffalo, NY

Key facts

Inspection ID 1326396
Firm ARTAFLEX BUFFALO INC
FEI number 3041244757
City Buffalo
State NY
ZIP 14216
Country United States
Fiscal year 2026
Inspection end date Jul 9, 2026
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

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

Browse all FDA inspections