FDA Inspection 1335198 — Przedsiebiorstwo Farmaceutyczne Jelfa SA

Przedsiebiorstwo Farmaceutyczne Jelfa SA — FEI 3004680543

The FDA completed an inspection of Przedsiebiorstwo Farmaceutyczne Jelfa SA on Mar 21, 2025 in Jelenia Gora. 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
Mar 21, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Jelenia Gora (Poland)

Additional Details

Mutual Recognition Agreement (MRA)

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