Neuronetrix Solutions, LLC
FDA inspection history in Louisville, Kentucky, 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 Louisville, Kentucky.
Cited most
Across all Neuronetrix Solutions observations on file
- 21 CFR 820.30(e)Design controls2
- 21 CFR 806.20(a)Records of corrections and removals not required to be reported1
- 21 CFR 820.100(b)Corrective and preventive action1
- 21 CFR 820.184Device history record1
- 21 CFR 820.198(c)Complaint files1
The complete Neuronetrix Solutions file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Louisville, Kentucky
One Form 483 · 2022 · 9 observations
Latest: Form 483, Nov 7, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-11-07 | 483 Form 483 | Louisville, Kentucky | 9 | $99 |
Investigators on these documents
FEI number 3011184129 · most recent document Nov 7, 2022
About Neuronetrix Solutions, LLC
How many FDA Form 483s has Neuronetrix Solutions, LLC received?
FDA Intel has 1 Form 483 on file for Neuronetrix Solutions, LLC; the most recent is dated Nov 7, 2022.
When was Neuronetrix Solutions, LLC last inspected by FDA?
The most recent FDA inspection document on file for Neuronetrix Solutions, LLC is a Form 483 dated Nov 7, 2022, for the site in Louisville, Kentucky.
What did FDA cite at Neuronetrix Solutions, LLC?
The regulations cited most in the observations on file for Neuronetrix Solutions, LLC are 21 CFR 820.30(e) (Design controls), 2 times; 21 CFR 806.20(a) (Records of corrections and removals not required to be reported), 1 time; 21 CFR 820.100(b) (Corrective and preventive action), 1 time.