FDA Inspection 1106846 — Beaumont Products Inc.

Beaumont Products Inc. — FEI 3000038524

The FDA completed an inspection of Beaumont Products Inc. on October 8, 2019 in Kennesaw, GA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 8, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kennesaw, GA (United States)