FDA Inspection 1227151 — Zolberg Corporation

Zolberg Corporation — FEI 3004200690

The FDA completed an inspection of Zolberg Corporation on Dec 7, 2023 in Cavite. 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
Dec 7, 2023
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Cavite (Philippines)

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