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FDA Inspection
•Evonik Active Oxygens, LLC•September 6, 2017

Evonik Active Oxygens, LLC – FDA Inspection, Sep 6, 2017

Record Details

This FDA Inspection record concerns Evonik Active Oxygens, LLC, with an inspection on September 6, 2017, issued by the Dallas District Office, covering human drugs.

Company
Evonik Active Oxygens, LLC
Inspection Date
September 6, 2017
Product Type
Human Drugs
Office
Dallas District Office
Person
  • Camerson E. Moore (FDA Associated Person)
View Company Profile

ID · 47f226d9-7b6b-4fd3-8542-ae23459060bb

Inspection Facts

Inspection number
1024999
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Evonik Active Oxygens, LLC

3
DateClassificationOfficeProject area
November 6, 2024Not classifiedDallas District Office
May 28, 2015NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 1, 2009NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Evonik Active Oxygens, LLC
  • FDA Inspection 1253963 - 2024-11-06
  • FDA Inspection 931423 - 2015-05-28
  • FDA Inspection 585330 - 2009-06-01

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