FDA inspection

Distron Corporation: FDA inspection ending Mar 15, 2018

FDA inspection 1045305 · No Action Indicated (NAI) · Attleboro Falls, MA

Key facts

Inspection ID 1045305
Firm Distron Corporation
FEI number 3006621944
Address 87 John L Dietsch Sq
City Attleboro Falls
State MA
ZIP 02763
Country United States
Fiscal year 2018
Inspection end date Mar 15, 2018
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

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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