ClinImmune Labs
FDA inspection history in Aurora, Colorado, 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, at Aurora, Colorado.
Cited most
Across all ClinImmune Labs observations on file
- 21 CFR 211.160General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.25Personnel qualifications1
- 21 CFR 211.28Personnel responsibilities1
- 21 CFR 211.42Design and construction features1
The complete ClinImmune Labs file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Aurora, Colorado
One Form 483 · 2019 · 7 observations
Latest: Form 483, Jul 19, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-07-19 | 483 Form 483 | Aurora, Colorado | 7 | $99 |
Investigators on these documents
FEI number 3000719146 · most recent document Jul 19, 2019
About ClinImmune Labs
How many FDA Form 483s has ClinImmune Labs received?
FDA Intel has 1 Form 483 on file for ClinImmune Labs; the most recent is dated Jul 19, 2019.
When was ClinImmune Labs last inspected by FDA?
The most recent FDA inspection document on file for ClinImmune Labs is a Form 483 dated Jul 19, 2019, for the site in Aurora, Colorado.
What did FDA cite at ClinImmune Labs?
The regulations cited most in the observations on file for ClinImmune Labs are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.25 (Personnel qualifications), 1 time.