Quest Products, LLC
FDA inspection history in Kent, Washington, 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 Kent, Washington.
Cited most
Across all Quest Products observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.188(a)Batch production and control records1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.63Equipment design, size, and location1
The complete Quest Products file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Kent, Washington
One Form 483 · 2024 · 6 observations
Latest: Form 483, Nov 7, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-11-07 | 483 Form 483 | Kent, Washington | 6 | $99 |
FEI number 3007802698 · most recent document Nov 7, 2024
About Quest Products, LLC
How many FDA Form 483s has Quest Products, LLC received?
FDA Intel has 1 Form 483 on file for Quest Products, LLC; the most recent is dated Nov 7, 2024.
When was Quest Products, LLC last inspected by FDA?
The most recent FDA inspection document on file for Quest Products, LLC is a Form 483 dated Nov 7, 2024, for the site in Kent, Washington.
What did FDA cite at Quest Products, LLC?
The regulations cited most in the observations on file for Quest Products, LLC are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.188(a) (Batch production and control records), 1 time.