FDA Inspection 1248213 — Clinical Resolution Laboratory Inc.

Clinical Resolution Laboratory Inc. — FEI 3005727243

The FDA completed an inspection of Clinical Resolution Laboratory Inc. on Aug 12, 2024 in Brea, 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). Product area: Food/Cosmetics.

Inspection Details

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.