American Red Cross Blood Services
FDA inspection history in Louisville, Kentucky, 2008
- 1
- Form 483
Every document, by year
- Form 483
2008: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2008One Form 483, at Louisville, Kentucky.
Cited most
Across all American Red Cross Blood Services observations on file
- 21 CFR 606.100Standard operating procedures4
- 21 CFR 606.171Reporting of product deviations by licensed manufacturers, unlicensed registered blood establishments, and transfusion services1
The complete American Red Cross Blood Services file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Louisville, Kentucky
One Form 483 · 2008 · 5 observations
Latest: Form 483, Apr 25, 2008 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2008-04-25 | 483 Form 483 | Louisville, Kentucky | 5 | $99 |
FEI number 1073003 · most recent document Apr 25, 2008
About American Red Cross Blood Services
How many FDA Form 483s has American Red Cross Blood Services received?
FDA Intel has 1 Form 483 on file for American Red Cross Blood Services; the most recent is dated Apr 25, 2008.
When was American Red Cross Blood Services last inspected by FDA?
The most recent FDA inspection document on file for American Red Cross Blood Services is a Form 483 dated Apr 25, 2008, for the site in Louisville, Kentucky.
What did FDA cite at American Red Cross Blood Services?
The regulations cited most in the observations on file for American Red Cross Blood Services are 21 CFR 606.100 (Standard operating procedures), 4 times; 21 CFR 606.171 (Reporting of product deviations by licensed manufacturers, unlicensed registered blood establishments, and transfusion services), 1 time.