by ComplianceQuest
My Dashboard
Inspection Tracker
FDA Guidance
Templates
Assessments
Sign in
Get started
Tracker Overview
Enforcement Themes
Form 483s
Warning Letters
Inspections
Recalls
Investigators
Companies
Facilities
Loading…
Dashboard
Warning Letters
Warning Letter Details
Asanuma Corporation - Sagamihara Factory Warning Letter Details
Warning Letter
Watch this company
View Letter
Overview
Violations
Related Form 483s
1
Related Inspections
2
Asanuma Corporation - Sagamihara Factory
Recipient Title General Manager Quality Assurance Department, 1 Chome 14-41 Nishihashimoto, Midori Sagamihara , Kanagawa Japan
Issue Date
June 02, 2026
FEI Number
3010960168
Violations
4
Country
Japan
Issuing Office
Center for Drug Evaluation and Research (CDER)
Product Type
Drugs
Status
Open
Subject
CGMP/OTC Finished Pharmaceuticals/Adulterated
Asanuma Corporation - Sagamihara Factory FDA Warning Letter, June 2, 2026