Polyconversions, Inc
FDA inspection history in Champaign, Illinois, 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 Champaign, Illinois.
Cited most
Across all Polyconversions 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 820.198(a)Complaint files1
- 21 CFR 820.50Purchasing controls1
- 21 CFR 820.75(a)Process validation1
The complete Polyconversions file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Champaign, Illinois
One Form 483 · 2019 · 6 observations
Latest: Form 483, Aug 7, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-08-07 | 483 Form 483 | Champaign, Illinois | 6 | $99 |
Investigators on these documents
FEI number 3001239227 · most recent document Aug 7, 2019
About Polyconversions, Inc
How many FDA Form 483s has Polyconversions, Inc received?
FDA Intel has 1 Form 483 on file for Polyconversions, Inc; the most recent is dated Aug 7, 2019.
When was Polyconversions, Inc last inspected by FDA?
The most recent FDA inspection document on file for Polyconversions, Inc is a Form 483 dated Aug 7, 2019, for the site in Champaign, Illinois.
What did FDA cite at Polyconversions, Inc?
The regulations cited most in the observations on file for Polyconversions, Inc 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 820.198(a) (Complaint files), 1 time.