Johns Hopkins, Bayview Medical Center, Human Subjects Committee
FDA inspection history in Baltimore, Maryland, 2001
- 1
- Form 483
Every document, by year
- Form 483
2001: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2001One Form 483, at Baltimore, Maryland.
Cited most
Across all Johns Hopkins, Bayview Medical Center, Human Subjects Committee observations on file
- 21 CFR 56.108IRB functions and operations2
- 21 CFR 56.115IRB records2
- 21 CFR 56.111Criteria for IRB approval of research1
The complete Johns Hopkins, Bayview Medical Center, Human Subjects Committee file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Baltimore, Maryland
One Form 483 · 2001 · 5 observations
Latest: Form 483, Sep 7, 2001 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2001-09-07 | 483 Form 483 | Baltimore, Maryland | 5 | $99 |
Investigators on these documents
FEI number 1120913 · most recent document Sep 7, 2001
About Johns Hopkins, Bayview Medical Center, Human Subjects Committee
How many FDA Form 483s has Johns Hopkins, Bayview Medical Center, Human Subjects Committee received?
FDA Intel has 1 Form 483 on file for Johns Hopkins, Bayview Medical Center, Human Subjects Committee; the most recent is dated Sep 7, 2001.
When was Johns Hopkins, Bayview Medical Center, Human Subjects Committee last inspected by FDA?
The most recent FDA inspection document on file for Johns Hopkins, Bayview Medical Center, Human Subjects Committee is a Form 483 dated Sep 7, 2001, for the site in Baltimore, Maryland.
What did FDA cite at Johns Hopkins, Bayview Medical Center, Human Subjects Committee?
The regulations cited most in the observations on file for Johns Hopkins, Bayview Medical Center, Human Subjects Committee are 21 CFR 56.108 (IRB functions and operations), 2 times; 21 CFR 56.115 (IRB records), 2 times; 21 CFR 56.111 (Criteria for IRB approval of research), 1 time.