FDA Inspection 1306826 — Linde, Inc.

Linde, Inc. — FEI 1832669

The FDA completed an inspection of Linde, Inc. on March 11, 2026 in La Porte, IN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 11, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
La Porte, IN (United States)