FDA inspection

Beaumont Products Inc.: FDA inspection ending Oct 8, 2019

FDA inspection 1106846 · No Action Indicated (NAI) · Kennesaw, GA

Key facts

Inspection ID 1106846
Firm Beaumont Products Inc.
FEI number 3000038524
Address 1560 Big Shanty Dr Nw
City Kennesaw
State GA
ZIP 30144
Country United States
Fiscal year 2020
Inspection end date Oct 8, 2019
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

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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