FDA Inspection 718933 — Lincare Inc

Lincare Inc — FEI 1000138237

The FDA completed an inspection of Lincare Inc on Mar 7, 2011 in Aurora, 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
Mar 7, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Aurora, MO (United States)