Source: FDA, document on file. FDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3011564121.
Observations1
Issue DateSeptember 29, 2017
StatusNo Warning Letter
Establishment TypeProducer of Sterile Drug Products
Related Inspections0
Establishment Details
Firm
Lincare, Inc.
Location
Arkansas, United States
FEI Number
3011564121
Establishment Type
Producer of Sterile Drug Products
Product Type
Drugs
Issue Date
September 29, 2017
Country
United States
Inspection History
We hold no FDA inspection matched to this establishment.
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