FDA Inspection 1251910 — Laboratorios Liconsa SAU

Laboratorios Liconsa SAU — FEI 3005508367

The FDA completed an inspection of Laboratorios Liconsa SAU on Jan 17, 2025 in Azuqueca De Henares. 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: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 17, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Azuqueca De Henares (Spain)

Additional details

Bioanalytical BA/BE

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