FDA Inspection 1232144 — Lonza Biologics, Inc.

Lonza Biologics, Inc. — FEI 3001451441

The FDA completed an inspection of Lonza Biologics, Inc. on Mar 7, 2024 in Portsmouth, NH. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Mar 7, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Portsmouth, NH (United States)

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