Hospira Inc.
FDA inspection history in Clayt o n, North Carolina, 2012
- 2
- Form 483s
Every document, by year
- Form 483
2012: two Form 483s.
The story so far
Built from the dates and citations on the documents themselves.
- 2012Two Form 483s, at Clayt o n, North Carolina.
- 2012The longest 483 on file: 6 observations over 3 pages at Clayt o n, North Carolina.
Cited most
Across all Hospira observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.166(a)(3)Stability testing1
- 21 CFR 211.192Production record review1
The complete Hospira file.
All 2 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
Clayt o n, North Carolina
Two Form 483s · 2012 · 7 observations
Latest: Form 483, Jul 26, 2012 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2012-07-26 | 483 Form 483 | Clayt o n, North Carolina | 6 | $99 |
| 2012-03-09 | 483 Form 483 | Clayt o n, North Carolina | 1 | $99 |
Investigators on these documents
FEI number 1048698 · most recent document Jul 26, 2012
About Hospira Inc.
How many FDA Form 483s has Hospira Inc. received?
FDA Intel has 2 Form 483s on file for Hospira Inc.; the most recent is dated Jul 26, 2012.
When was Hospira Inc. last inspected by FDA?
The most recent FDA inspection document on file for Hospira Inc. is a Form 483 dated Jul 26, 2012, for the site in Clayt o n, North Carolina.
What did FDA cite at Hospira Inc.?
The regulations cited most in the observations on file for Hospira Inc. are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.160(b) (General requirements), 1 time.