NucleusHealth, LLC
FDA inspection history in San Diego, California, 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 San Diego, California.
Cited most
Across all NucleusHealth observations on file
- 21 CFR 820.181Device master record1
- 21 CFR 820.25(b)Personnel1
- 21 CFR 820.30(c)Design controls1
The complete NucleusHealth file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
San Diego, California
One Form 483 · 2019 · 3 observations
Latest: Form 483, Oct 30, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-10-30 | 483 Form 483 | San Diego, California | 3 | $99 |
Investigators on these documents
FEI number 3008008144 · most recent document Oct 30, 2019
About NucleusHealth, LLC
How many FDA Form 483s has NucleusHealth, LLC received?
FDA Intel has 1 Form 483 on file for NucleusHealth, LLC; the most recent is dated Oct 30, 2019.
When was NucleusHealth, LLC last inspected by FDA?
The most recent FDA inspection document on file for NucleusHealth, LLC is a Form 483 dated Oct 30, 2019, for the site in San Diego, California.
What did FDA cite at NucleusHealth, LLC?
The regulations cited most in the observations on file for NucleusHealth, LLC are 21 CFR 820.181 (Device master record), 1 time; 21 CFR 820.25(b) (Personnel), 1 time; 21 CFR 820.30(c) (Design controls), 1 time.