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FDA Inspection
•Dynavax GmbH•March 5, 2019

Dynavax GmbH – FDA Inspection, Mar 5, 2019

Record Details

This FDA Inspection record concerns Dynavax GmbH, with an inspection on March 5, 2019, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Dynavax GmbH
Inspection Date
March 5, 2019
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
People
  • Marian Major (Issuing Officer)
  • Omotunde O. Osunsanmi (Issuing Officer)
View Company Profile

ID · a8c35179-518c-40c2-aeb5-638214eaf10b

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1084951
FDA center
Biologics
Project area
Vaccines and Allergenic Products
Outcome
Form 483 issued

Other FDA inspections of Dynavax GmbH

1
DateClassificationOfficeProject area
February 3, 2023VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
Other documents for Dynavax GmbH
  • FDA Inspection 1201864 - 2023-02-03

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