FDA Inspection 1249142 — LANXESS Corporation

LANXESS Corporation — FEI 3022820

The FDA completed an inspection of LANXESS Corporation on Sep 12, 2024 in Kalama, WA. 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
Sep 12, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kalama, WA (United States)