FDA Inspection 843860 — Lincare Inc.

Lincare Inc. — FEI 1000512366

The FDA completed an inspection of Lincare Inc. on Aug 9, 2013 in Baltimore, MD. 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). 3 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 9, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Baltimore, MD (United States)

Citations

IDCFRDescription
111121 CFR 211.25(a)Training , Education , Experience overall
121521 CFR 211.67(b)Written procedures not established/followed
438621 CFR 211.198(b)Written complaint record to be maintained at facility