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FDA Inspection 991587 — Lonza Walkersville, Inc.

Lonza Walkersville, Inc. — FEI 1114298

The FDA completed an inspection of Lonza Walkersville, Inc. on June 9, 2016 in Walkersville, MD. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 9, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Walkersville, MD (United States)

Facility

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Recent compliance actions

FDA data resources