FDA Inspection 856011 — Linde Inc.

Linde Inc. — FEI 1921174

The FDA completed an inspection of Linde Inc. on Oct 24, 2013 in Kansas City, MO. 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
Oct 24, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kansas City, MO (United States)