KedPlasma LLC
FDA inspection history on file, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483.
Cited most
Across all KedPlasma observations on file
- 21 CFR 606.100Standard operating procedures1
- 21 CFR 630.40Requirements for notifying deferred donors1
The complete KedPlasma file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-03-21 | 483 Form 483 | — | 2 | $99 |
Investigators on these documents
Christopher Cox (1)Cordelia J. Brammer (1)Judy E. Ciaraldi (1)
FEI number 3014545171 · most recent document Mar 21, 2019
About KedPlasma LLC
How many FDA Form 483s has KedPlasma LLC received?
FDA Intel has 1 Form 483 on file for KedPlasma LLC; the most recent is dated Mar 21, 2019.
When was KedPlasma LLC last inspected by FDA?
The most recent FDA inspection document on file for KedPlasma LLC is a Form 483 dated Mar 21, 2019.
What did FDA cite at KedPlasma LLC?
The regulations cited most in the observations on file for KedPlasma LLC are 21 CFR 606.100 (Standard operating procedures), 1 time; 21 CFR 630.40 (Requirements for notifying deferred donors), 1 time.