FDA Inspection 1335784 — Clarochem Ireland Ltd.

Clarochem Ireland Ltd. — FEI 3010166641

The FDA completed an inspection of Clarochem Ireland Ltd. on Jan 31, 2025 in Dublin 15. 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 31, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dublin 15 (Ireland)

Additional Details

Mutual Recognition Agreement (MRA)

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