Heartland I.V. Care
FDA inspection history in Saint Paul, Minnesota, 2017
- 1
- Form 483
Every document, by year
- Form 483
2017: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at Saint Paul, Minnesota.
Cited most
Across all Heartland I.V. Care observations on file
- 21 CFR 211.113Control of microbiological contamination1
The complete Heartland I.V. Care file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Saint Paul, Minnesota
One Form 483 · 2017 · 1 observation
Latest: Form 483, Jul 14, 2017 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2017-07-14 | 483 Form 483 | Saint Paul, Minnesota | 1 | $99 |
Investigators on these documents
FEI number 3013576855 · most recent document Jul 14, 2017
About Heartland I.V. Care
How many FDA Form 483s has Heartland I.V. Care received?
FDA Intel has 1 Form 483 on file for Heartland I.V. Care; the most recent is dated Jul 14, 2017.
When was Heartland I.V. Care last inspected by FDA?
The most recent FDA inspection document on file for Heartland I.V. Care is a Form 483 dated Jul 14, 2017, for the site in Saint Paul, Minnesota.
What did FDA cite at Heartland I.V. Care?
The regulations cited most in the observations on file for Heartland I.V. Care are 21 CFR 211.113 (Control of microbiological contamination), 1 time.