FDA Inspection 922552 — Lincare Inc.

Lincare Inc. — FEI 3002726192

The FDA completed an inspection of Lincare Inc. on Apr 16, 2015 in Saint Paul, MN. 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
Apr 16, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saint Paul, MN (United States)