Hillyard GMP
FDA inspection history in Saint Joseph, Missouri, 2021 to 2026
- 2
- Form 483s
Every document, by year
- Form 483
2021: one Form 483; 2026: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2021One Form 483, at Saint Joseph, Missouri.
- 2026One Form 483, at Saint Joseph, Missouri.
- 2026The longest 483 on file: 1 observation over 3 pages at Saint Joseph, Missouri.
Cited most
Across all Hillyard GMP observations on file
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Hillyard GMP file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Saint Joseph, Missouri
Two Form 483s · 2021 to 2026 · 2 observations
Latest: Form 483, Feb 27, 2026 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-02-27 | 483 Form 483 | Saint Joseph, Missouri | 1 | $99 |
| 2021-10-08 | 483 Form 483 | Saint Joseph, Missouri | 1 | $99 |
Investigators on these documents
Aerial A. Smith (1)Carl A. Huffman (1)Eric D. Bowles (1)Gretchen L. Trendel (1)
FEI number 3009690111 · most recent document Feb 27, 2026
About Hillyard GMP
How many FDA Form 483s has Hillyard GMP received?
FDA Intel has 2 Form 483s on file for Hillyard GMP; the most recent is dated Feb 27, 2026.
When was Hillyard GMP last inspected by FDA?
The most recent FDA inspection document on file for Hillyard GMP is a Form 483 dated Feb 27, 2026, for the site in Saint Joseph, Missouri.
What did FDA cite at Hillyard GMP?
The regulations cited most in the observations on file for Hillyard GMP are 21 CFR 211.160(b) (General requirements), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.