Hatch Product Development LLC
FDA inspection history in Waukegan, Illinois, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483, at Waukegan, Illinois.
Cited most
Across all Hatch Product Development observations on file
- 21 CFR 803.17What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?1
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.198(a)Complaint files1
- 21 CFR 820.80(d)Receiving, in-process, and finished device acceptance1
- 21 CFR 820.90(a)Nonconforming product1
The complete Hatch Product Development file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Waukegan, Illinois
One Form 483 · 2025 · 5 observations
Latest: Form 483, Dec 11, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-12-11 | 483 Form 483 | Waukegan, Illinois | 5 | $99 |
FEI number 3030438338 · most recent document Dec 11, 2025
About Hatch Product Development LLC
How many FDA Form 483s has Hatch Product Development LLC received?
FDA Intel has 1 Form 483 on file for Hatch Product Development LLC; the most recent is dated Dec 11, 2025.
When was Hatch Product Development LLC last inspected by FDA?
The most recent FDA inspection document on file for Hatch Product Development LLC is a Form 483 dated Dec 11, 2025, for the site in Waukegan, Illinois.
What did FDA cite at Hatch Product Development LLC?
The regulations cited most in the observations on file for Hatch Product Development LLC are 21 CFR 803.17 (What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?), 1 time; 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.198(a) (Complaint files), 1 time.