FDA Inspection 1227553 — Triclinic Labs, Inc.

Triclinic Labs, Inc. — FEI 3007799585

The FDA completed an inspection of Triclinic Labs, Inc. on Jan 17, 2024 in Lafayette, IN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 17, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lafayette, IN (United States)