Humacyte Global, Inc
FDA inspection history in Durham, North Carolina, 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 Durham, North Carolina.
Cited most
Across all Humacyte Global observations on file
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.192Production record review1
- 21 CFR 211.25Personnel qualifications1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Humacyte Global file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Durham, North Carolina
One Form 483 · 2024 · 2 observations
Latest: Form 483, Apr 5, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-04-05 | 483 Form 483 | Durham, North Carolina | 2 | $99 |
Investigators on these documents
Alifiya H. Ghadiali (1)Jin Sung Hong (1)Laura Ricles (1)Zainab Mansaray-Stonns (1)
FEI number 3014294024 · most recent document Apr 5, 2024
About Humacyte Global, Inc
How many FDA Form 483s has Humacyte Global, Inc received?
FDA Intel has 1 Form 483 on file for Humacyte Global, Inc; the most recent is dated Apr 5, 2024.
When was Humacyte Global, Inc last inspected by FDA?
The most recent FDA inspection document on file for Humacyte Global, Inc is a Form 483 dated Apr 5, 2024, for the site in Durham, North Carolina.
What did FDA cite at Humacyte Global, Inc?
The regulations cited most in the observations on file for Humacyte Global, Inc are 21 CFR 211.22 (Responsibilities of quality control unit), 2 times; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.25 (Personnel qualifications), 1 time.