CellTrans Inc.
FDA inspection history in Chicago, Illinois, 2021
- 1
- Form 483
Every document, by year
- Form 483
2021: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2021One Form 483, at Chicago, Illinois.
Cited most
Across all CellTrans observations on file
- 21 CFR 211.113Control of microbiological contamination3
- 21 CFR 211.192Production record review2
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.67Equipment cleaning and maintenance2
- 21 CFR 211.165Testing and release for distribution1
The complete CellTrans file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Chicago, Illinois
One Form 483 · 2021
Latest: Form 483, Jun 11, 2021 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2021-06-11 | 483 Form 483 | Chicago, Illinois | — | $99 |
FEI number 3019202665 · most recent document Jun 11, 2021
About CellTrans Inc.
How many FDA Form 483s has CellTrans Inc. received?
FDA Intel has 1 Form 483 on file for CellTrans Inc.; the most recent is dated Jun 11, 2021.
When was CellTrans Inc. last inspected by FDA?
The most recent FDA inspection document on file for CellTrans Inc. is a Form 483 dated Jun 11, 2021, for the site in Chicago, Illinois.
What did FDA cite at CellTrans Inc.?
The regulations cited most in the observations on file for CellTrans Inc. are 21 CFR 211.113 (Control of microbiological contamination), 3 times; 21 CFR 211.192 (Production record review), 2 times; 21 CFR 211.22 (Responsibilities of quality control unit), 2 times.