American Red Cross Greater Alleghenies Regio
FDA inspection history in Johnstown, Pennsylvania, 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 Johnstown, Pennsylvania.
- 2010The longest 483 on file: 5 observations over 5 pages at Johnstown, Pennsylvania.
Cited most
Across all American Red Cross Greater Alleghenies Regio observations on file
- 21 CFR 211.192Production record review2
- 21 CFR 606.100Standard operating procedures2
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 606.170(a)Adverse reaction file1
- 21 CFR 606.20(b)Personnel1
The complete American Red Cross Greater Alleghenies Regio 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
Johnstown, Pennsylvania
Two Form 483s · 2008 to 2010 · 8 observations
Latest: Form 483, Sep 24, 2010 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2010-09-24 | 483 Form 483 | Johnstown, Pennsylvania | 5 | $99 |
| 2008-09-16 | 483 Form 483 | Johnstown, Pennsylvania | 3 | $99 |
Investigators on these documents
FEI number 2573016 · most recent document Sep 24, 2010
About American Red Cross Greater Alleghenies Regio
How many FDA Form 483s has American Red Cross Greater Alleghenies Regio received?
FDA Intel has 2 Form 483s on file for American Red Cross Greater Alleghenies Regio; the most recent is dated Sep 24, 2010.
When was American Red Cross Greater Alleghenies Regio last inspected by FDA?
The most recent FDA inspection document on file for American Red Cross Greater Alleghenies Regio is a Form 483 dated Sep 24, 2010, for the site in Johnstown, Pennsylvania.
What did FDA cite at American Red Cross Greater Alleghenies Regio?
The regulations cited most in the observations on file for American Red Cross Greater Alleghenies Regio are 21 CFR 211.192 (Production record review), 2 times; 21 CFR 606.100 (Standard operating procedures), 2 times; 21 CFR 211.100(a) (Written procedures; deviations), 1 time.