FDA Warning Letter — Lonza Walkersville, Inc.

Case 520239 — FEI 1114298

The FDA took a Warning Letter action against Lonza Walkersville, Inc. on April 21, 2017 (Walkersville, MD). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Lonza Walkersville, Inc.
Date
April 21, 2017
Fiscal Year
2017
Product Type
Devices
Center
CDRH
Location
Walkersville, MD (United States)