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FDA Inspection
•FinVector Oy•May 28, 2024

FinVector Oy – FDA Inspection, May 28, 2024

Record Details

This FDA Inspection record concerns FinVector Oy, with an inspection on May 28, 2024, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
FinVector Oy
Inspection Date
May 28, 2024
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
People
  • Gene D. Arcy
  • Lewis K. Antwi (Issuing Officer)
View Company Profile

ID · 2c9beb12-0213-49b0-a4a4-80033db8bbe8

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1239622
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

FDA Citations

3
  1. 21 CFR 211.84(d)(3)Establish reliability of supplier's C of A
  2. 21 CFR 211.22(c)Approve or reject procedures or specs
  3. 21 CFR 211.67(b)Written procedures fail to include

Full citation text and observation details available on the Dashboard.

Other FDA inspections of FinVector Oy

1
DateClassificationOfficeProject area
March 4, 2026Not classifiedOffice of Inspections and Investigations
Other documents for FinVector Oy
  • FDA Inspection 1309498 - 2026-03-04

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