Carolina Biological Supply Co
FDA inspection history in Burlington, North Carolina, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Burlington, North Carolina.
Cited most
Across all Carolina Biological Supply observations on file
- 21 CFR 803.17What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?1
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.22Quality audit1
- 21 CFR 820.25(b)Personnel1
- 21 CFR 820.40(a)Document controls1
The complete Carolina Biological Supply file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Burlington, North Carolina
One Form 483 · 2022 · 6 observations
Latest: Form 483, Sep 23, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-09-23 | 483 Form 483 | Burlington, North Carolina | 6 | $99 |
Investigators on these documents
FEI number 1000111286 · most recent document Sep 23, 2022
About Carolina Biological Supply Co
How many FDA Form 483s has Carolina Biological Supply Co received?
FDA Intel has 1 Form 483 on file for Carolina Biological Supply Co; the most recent is dated Sep 23, 2022.
When was Carolina Biological Supply Co last inspected by FDA?
The most recent FDA inspection document on file for Carolina Biological Supply Co is a Form 483 dated Sep 23, 2022, for the site in Burlington, North Carolina.
What did FDA cite at Carolina Biological Supply Co?
The regulations cited most in the observations on file for Carolina Biological Supply Co are 21 CFR 803.17 (What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?), 1 time; 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.22 (Quality audit), 1 time.