FDA inspection

Distron Corporation: FDA inspection ending Mar 20, 2024

FDA inspection 1234273 · Voluntary Action Indicated (VAI) · Attleboro Falls, MA

Key facts

Inspection ID 1234273
Firm Distron Corporation
FEI number 3006621944
Address 87 John L Dietsch Sq
City Attleboro Falls
State MA
ZIP 02763
Country United States
Fiscal year 2024
Inspection end date Mar 20, 2024
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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

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