Heartland I.V. Care

Form 483

Minnesota, United StatesFEI 3013576855Issued August 21, 2017

View Form 483 PDF

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 3013576855.

Observations1

Issue DateAugust 21, 2017

StatusNo Warning Letter

Establishment TypeProducer of Sterile Drug Products

Related Inspections0

Establishment Details

Firm: Heartland I.V. Care
Location: Minnesota, United States
FEI Number: 3013576855
Establishment Type: Producer of Sterile Drug Products
Product Type: Drugs
Issue Date: August 21, 2017
Country: United States

Inspection History

We hold no FDA inspection matched to this establishment.

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Heartland I.V. Care FDA Form 483, Minnesota, August 21, 2017