FDA Warning Letter — Viatris, Inc.

Case 557903 — FEI 1110315

The FDA took a Warning Letter action against Viatris, Inc. on Nov 9, 2018 (Morgantown, WV). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Viatris, Inc.
Date
Nov 9, 2018
Fiscal Year
2019
Product Type
Drugs
Center
CDER
Location
Morgantown, WV (United States)

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