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FDA Inspection
•Hirotaka Nagashima•December 12, 2025

FDA Inspection 1296482 - Hirotaka Nagashima - December 12, 2025

Record Details

This FDA Inspection record concerns Hirotaka Nagashima, with an inspection on December 12, 2025, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Hirotaka Nagashima
Inspection Date
December 12, 2025
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Raman K. Kaushal (Issuing Officer)
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ID · 767a5ab0-0019-48a9-bbe3-bf9a964eced7

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1296482
FDA center
Human Drugs
Project area
Bioresearch Monitoring: Human Drugs
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 312.62(b)Case history records- inadequate or inadequate

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