American National Red Cross Great Lakes Region
FDA inspection history in Lansing, Michigan, 2008 to 2010
- 2
- Form 483s
Every document, by year
- Form 483
2008: one Form 483; 2010: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2008–10Two Form 483s, at Lansing, Michigan.
- 2008The longest 483 on file: 4 observations over 3 pages at Lansing, Michigan.
Cited most
Across all American National Red Cross Great Lakes Region observations on file
- 21 CFR 606.100Standard operating procedures5
- 21 CFR 606.170(a)Adverse reaction file1
- 21 CFR 606.171Reporting of product deviations by licensed manufacturers, unlicensed registered blood establishments, and transfusion services1
The complete American National Red Cross Great Lakes Region 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
Lansing, Michigan
Two Form 483s · 2008 to 2010 · 6 observations
Latest: Form 483, Apr 27, 2010 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2010-04-27 | 483 Form 483 | Lansing, Michigan | 2 | $99 |
| 2008-03-21 | 483 Form 483 | Lansing, Michigan | 4 | $99 |
Investigators on these documents
FEI number 1873033 · most recent document Apr 27, 2010
About American National Red Cross Great Lakes Region
How many FDA Form 483s has American National Red Cross Great Lakes Region received?
FDA Intel has 2 Form 483s on file for American National Red Cross Great Lakes Region; the most recent is dated Apr 27, 2010.
When was American National Red Cross Great Lakes Region last inspected by FDA?
The most recent FDA inspection document on file for American National Red Cross Great Lakes Region is a Form 483 dated Apr 27, 2010, for the site in Lansing, Michigan.
What did FDA cite at American National Red Cross Great Lakes Region?
The regulations cited most in the observations on file for American National Red Cross Great Lakes Region are 21 CFR 606.100 (Standard operating procedures), 5 times; 21 CFR 606.170(a) (Adverse reaction file), 1 time; 21 CFR 606.171 (Reporting of product deviations by licensed manufacturers, unlicensed registered blood establishments, and transfusion services), 1 time.