FDA Inspection 1060952 — Lincare, Inc

Lincare, Inc — FEI 3000215120

The FDA completed an inspection of Lincare, Inc on Jul 12, 2018 in Lamar, CO. 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
Jul 12, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lamar, CO (United States)