FDA Warning Letter — EyePoint US, Inc.

Case 679747 — FEI 3005508657

The FDA took a Warning Letter action against EyePoint US, Inc. on July 12, 2024 (Watertown, MA). The action was issued by CDER and concerns drugs products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
EyePoint US, Inc.
Date
July 12, 2024
Fiscal Year
2024
Product Type
Drugs
Center
CDER
Location
Watertown, MA (United States)