FDA Inspection 1007877 — Dexcel Ltd.

Dexcel Ltd. — FEI 3002806801

The FDA completed an inspection of Dexcel Ltd. on Feb 16, 2017 in Or Akiva. 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
Feb 16, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Or Akiva (Israel)

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