FDA Warning Letter — Bentley Laboratories LLC

Case 732028 — FEI 2244819

The FDA took a Warning Letter action against Bentley Laboratories LLC on Sep 17, 2026 (Edison, NJ). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Bentley Laboratories LLC
Date
Sep 17, 2026
Fiscal Year
2026
Product Type
Drugs
Center
CDER
Location
Edison, NJ (United States)

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