Solomon Park Research Laboratories, Inc.
FDA inspection history in Burien, Washington, 2026
- 1
- Form 483
Every document, by year
- Form 483
2026: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2026One Form 483, at Burien, Washington.
Cited most
Across all Solomon Park Research Laboratories observations on file
- 21 CFR 8301
- 21 CFR 803.17What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?1
- 21 CFR 820.90(b)(1)Nonconforming product1
The complete Solomon Park Research Laboratories file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Burien, Washington
One Form 483 · 2026 · 3 observations
Latest: Form 483, Jan 8, 2026 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-01-08 | 483 Form 483 | Burien, Washington | 3 | $99 |
Investigators on these documents
FEI number 3023437 · most recent document Jan 8, 2026
About Solomon Park Research Laboratories, Inc.
How many FDA Form 483s has Solomon Park Research Laboratories, Inc. received?
FDA Intel has 1 Form 483 on file for Solomon Park Research Laboratories, Inc.; the most recent is dated Jan 8, 2026.
When was Solomon Park Research Laboratories, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Solomon Park Research Laboratories, Inc. is a Form 483 dated Jan 8, 2026, for the site in Burien, Washington.
What did FDA cite at Solomon Park Research Laboratories, Inc.?
The regulations cited most in the observations on file for Solomon Park Research Laboratories, Inc. are 21 CFR 830, 1 time; 21 CFR 803.17 (What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?), 1 time; 21 CFR 820.90(b)(1) (Nonconforming product), 1 time.