Hospira Boulder, Inc.
FDA inspection history in Lake Forest, Illinois, 2012 to 2015
- 3
- Form 483s
Every document, by year
- Form 483
2012: one Form 483; 2013: one Form 483; 2015: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2012–15Three Form 483s, at Lake Forest, Illinois.
- 2013The longest 483 on file: 10 observations over 9 pages at Lake Forest, Illinois.
Cited most
Across all Hospira Boulder observations on file
- 21 CFR 820.100Corrective and preventive action7
- 21 CFR 820.30Design controls5
- 21 CFR 820.198Complaint files4
- 21 CFR 803.52If I am a manufacturer, what information must I submit in my individual adverse event reports?2
- 21 CFR 820.50Purchasing controls2
The complete Hospira Boulder file.
All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Lake Forest, Illinois
Three Form 483s · 2012 to 2015 · 24 observations
Latest: Form 483, May 27, 2015 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-05-27 | 483 Form 483 | Lake Forest, Illinois | 4 | $99 |
| 2013-02-07 | 483 Form 483 | Lake Forest, Illinois | 10 | $99 |
| 2012-07-13 | 483 Form 483 | Lake Forest, Illinois | 10 | $99 |
Investigators on these documents
Jesse A. Vazquez (1)Phillip M. Pontikos (1)Rafael Padilla (1)Sean T. Creighton (1)Tonnie L. Carter (1)
FEI number 3005579246 · most recent document May 27, 2015
About Hospira Boulder, Inc.
How many FDA Form 483s has Hospira Boulder, Inc. received?
FDA Intel has 3 Form 483s on file for Hospira Boulder, Inc.; the most recent is dated May 27, 2015.
When was Hospira Boulder, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Hospira Boulder, Inc. is a Form 483 dated May 27, 2015, for the site in Lake Forest, Illinois.
What did FDA cite at Hospira Boulder, Inc.?
The regulations cited most in the observations on file for Hospira Boulder, Inc. are 21 CFR 820.100 (Corrective and preventive action), 7 times; 21 CFR 820.30 (Design controls), 5 times; 21 CFR 820.198 (Complaint files), 4 times.