FDA Inspection 902816 — Catalent U.K. Packaging Limited

Catalent U.K. Packaging Limited — FEI 3002808428

The FDA completed an inspection of Catalent U.K. Packaging Limited on Oct 14, 2014 in Bolton. 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
Oct 14, 2014
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bolton (United Kingdom)

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