FDA Inspection 720038 — Lincare, Inc.

Lincare, Inc. — FEI 1000113164

The FDA completed an inspection of Lincare, Inc. on Apr 14, 2011 in Melbourne, FL. 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
Apr 14, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Melbourne, FL (United States)