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FDA Inspection
•Heraeus Deutschland GmbH & Co. KG•May 18, 2018

Heraeus Deutschland GmbH & Co. KG – FDA Inspection, May 18, 2018

Record Details

This FDA Inspection record concerns Heraeus Deutschland GmbH & Co. KG, with an inspection on May 18, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Heraeus Deutschland GmbH & Co. KG
Inspection Date
May 18, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Robert J. Ham (FDA Associated Person)
View Company Profile

ID · a00005f8-a4da-4ff0-937a-0aa2fa86d8d1

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1055814
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Heraeus Deutschland GmbH & Co. KG

3
DateClassificationOfficeProject area
August 5, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 7, 2014NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 4, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Heraeus Deutschland GmbH & Co. KG
  • FDA Inspection 1289120 - 2022-08-05
  • FDA Inspection 870083 - 2014-03-07
  • FDA Inspection 654545 - 2010-03-04

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