FDA Inspection 1248213 — Clinical Resolution Laboratory Inc.

Clinical Resolution Laboratory Inc. — FEI 3005727243

The FDA completed an inspection of Clinical Resolution Laboratory Inc. on August 12, 2024 in Brea, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 12, 2024
Fiscal Year
2024
Product Type
Food/Cosmetics
Project Area
Colors and Cosmetics Technology
Location
Brea, CA (United States)