FDA Inspection 940336 — Cilag AG

Cilag AG — FEI 3002806695

The FDA completed an inspection of Cilag AG on Sep 8, 2015 in Schaffhausen. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Sep 8, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Schaffhausen (Switzerland)

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