FDA Inspection 1239756 — Lykos Therapeutics, Inc.

Lykos Therapeutics, Inc. — FEI 3025253687

The FDA completed an inspection of Lykos Therapeutics, Inc. on May 15, 2024 in Santa Cruz, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 15, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Santa Cruz, CA (United States)

Additional Details

Sponsor, Contract Research Organization

Citations

IDCFRDescription
748221 CFR 312.50General responsibilities of sponsors