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FDA Inspection
•Nitto Denko Avecia Inc.•February 8, 2023

Nitto Denko Avecia Inc. – FDA Inspection, Feb 8, 2023

Record Details

This FDA Inspection record concerns Nitto Denko Avecia Inc., with an inspection on February 8, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Nitto Denko Avecia Inc.
Inspection Date
February 8, 2023
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Erik W. Koester (FDA Associated Person)
View Company Profile

ID · dae811af-bbba-4c86-9c1d-2bf6e29e97fa

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1196842
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Nitto Denko Avecia Inc.

3
DateClassificationOfficeProject area
August 12, 2026NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 10, 2018Not classifiedNew England District Office
November 24, 2008NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Nitto Denko Avecia Inc.
  • FDA Inspection 1300758 - 2026-08-12
  • FDA Inspection 1052825 - 2018-05-10
  • FDA Inspection 553036 - 2008-11-24

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