FDA Inspection 1228229 — Changzhou Pharmaceutical Factory

Changzhou Pharmaceutical Factory — FEI 3002806661

The FDA completed an inspection of Changzhou Pharmaceutical Factory on Jan 12, 2024 in Changzhou. 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 12, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Changzhou (China)

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