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
Simtra BioPharma Solutions Warning Letter Details
Warning Letter
Watch this company
View Letter
Overview
Violations
Related Form 483s
5
Related Inspections
10
Simtra BioPharma Solutions
Building C, Suite 270, 2nd Floor 400 Interpace Parkway Parsippany , NJ 07054 United States
Issue Date
March 03, 2026
FEI Number
3002806419
Violations
2
Country
United States
Issuing Office
Center for Drug Evaluation and Research (CDER)
Product Type
Drugs
Status
Open
Subject
CGMP/Finished Pharmaceuticals/Adulterated
Simtra BioPharma Solutions FDA Warning Letter, March 3, 2026