FDA Inspection 1224900 — Vee Pak LLC

Vee Pak LLC — FEI 1421421

The FDA completed an inspection of Vee Pak LLC on Dec 11, 2023 in Countryside, IL. 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
Dec 11, 2023
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Countryside, IL (United States)

Citations

IDCFRDescription
192021 CFR 211.166(a)(3)Valid stability test methods

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