Quadric BioMed, LLC
FDA inspection history in Colorado Springs, Colorado, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Colorado Springs, Colorado.
Cited most
Across all Quadric BioMed observations on file
- 21 CFR 820.20(c)Management responsibility1
- 21 CFR 820.22Quality audit1
- 21 CFR 820.25(b)Personnel1
- 21 CFR 820.50Purchasing controls1
The complete Quadric BioMed file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Colorado Springs, Colorado
One Form 483 · 2024 · 4 observations
Latest: Form 483, Dec 16, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-12-16 | 483 Form 483 | Colorado Springs, Colorado | 4 | $99 |
Investigators on these documents
FEI number 3025467473 · most recent document Dec 16, 2024
About Quadric BioMed, LLC
How many FDA Form 483s has Quadric BioMed, LLC received?
FDA Intel has 1 Form 483 on file for Quadric BioMed, LLC; the most recent is dated Dec 16, 2024.
When was Quadric BioMed, LLC last inspected by FDA?
The most recent FDA inspection document on file for Quadric BioMed, LLC is a Form 483 dated Dec 16, 2024, for the site in Colorado Springs, Colorado.
What did FDA cite at Quadric BioMed, LLC?
The regulations cited most in the observations on file for Quadric BioMed, LLC are 21 CFR 820.20(c) (Management responsibility), 1 time; 21 CFR 820.22 (Quality audit), 1 time; 21 CFR 820.25(b) (Personnel), 1 time.