FDA Inspection 1330228 — Frontage Laboratories, Inc.

Frontage Laboratories, Inc. — FEI 3006799640

The FDA completed an inspection of Frontage Laboratories, Inc. on Jun 18, 2026 in Exton, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 18, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Exton, PA (United States)

Additional Details

Bioanalytical BA/BE

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