FDA Inspection 1298600 — Solesence, Inc.

Solesence, Inc. — FEI 3003574860

The FDA completed an inspection of Solesence, Inc. on January 9, 2026 in Romeoville, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 9, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Romeoville, IL (United States)