Noble Panacea Labs, Inc
FDA inspection history in Irvine, California, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Irvine, California.
Cited most
Across all Noble Panacea Labs observations on file
- 21 CFR 211.160(b)General requirements2
- 21 CFR 211.22(c)Responsibilities of quality control unit2
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.166(a)Stability testing1
- 21 CFR 211.170(b)Reserve samples1
The complete Noble Panacea Labs file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Irvine, California
One Form 483 · 2024 · 11 observations
Latest: Form 483, Nov 8, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-11-08 | 483 Form 483 | Irvine, California | 11 | $99 |
Investigators on these documents
FEI number 3027485555 · most recent document Nov 8, 2024
About Noble Panacea Labs, Inc
How many FDA Form 483s has Noble Panacea Labs, Inc received?
FDA Intel has 1 Form 483 on file for Noble Panacea Labs, Inc; the most recent is dated Nov 8, 2024.
When was Noble Panacea Labs, Inc last inspected by FDA?
The most recent FDA inspection document on file for Noble Panacea Labs, Inc is a Form 483 dated Nov 8, 2024, for the site in Irvine, California.
What did FDA cite at Noble Panacea Labs, Inc?
The regulations cited most in the observations on file for Noble Panacea Labs, Inc are 21 CFR 211.160(b) (General requirements), 2 times; 21 CFR 211.22(c) (Responsibilities of quality control unit), 2 times; 21 CFR 211.100(a) (Written procedures; deviations), 1 time.