Myerson LLC
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 Myerson observations on file
- 21 CFR 803.50(a)(1)If I am a manufacturer, what reporting requirements apply to me?2
- 21 CFR 820.30(g)Design controls2
- 21 CFR 8201
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.184Device history record1
The complete Myerson file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Chicago, Illinois
One Form 483 · 2021 · 8 observations
Latest: Form 483, May 4, 2021 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2021-05-04 | 483 Form 483 | Chicago, Illinois | 8 | $99 |
Investigators on these documents
FEI number 3003928050 · most recent document May 4, 2021
About Myerson LLC
How many FDA Form 483s has Myerson LLC received?
FDA Intel has 1 Form 483 on file for Myerson LLC; the most recent is dated May 4, 2021.
When was Myerson LLC last inspected by FDA?
The most recent FDA inspection document on file for Myerson LLC is a Form 483 dated May 4, 2021, for the site in Chicago, Illinois.
What did FDA cite at Myerson LLC?
The regulations cited most in the observations on file for Myerson LLC are 21 CFR 803.50(a)(1) (If I am a manufacturer, what reporting requirements apply to me?), 2 times; 21 CFR 820.30(g) (Design controls), 2 times; 21 CFR 820, 1 time.