HK INNO.N CORPORATION
FDA inspection history in Heungbeok Cheongju, South Korea, 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 Heungbeok Cheongju, South Korea.
Cited most
Across all HK INNO.N observations on file
- 21 CFR 211.113Control of microbiological contamination2
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.122Materials examination and usage criteria1
- 21 CFR 211.160General requirements1
- 21 CFR 211.165Testing and release for distribution1
The complete HK INNO.N file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Heungbeok Cheongju, South Korea
One Form 483 · 2025 · 11 observations
Latest: Form 483, Jan 24, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-01-24 | 483 Form 483 | Heungbeok Cheongju, South Korea | 11 | $99 |
FEI number 3022306074 · most recent document Jan 24, 2025
About HK INNO.N CORPORATION
How many FDA Form 483s has HK INNO.N CORPORATION received?
FDA Intel has 1 Form 483 on file for HK INNO.N CORPORATION; the most recent is dated Jan 24, 2025.
When was HK INNO.N CORPORATION last inspected by FDA?
The most recent FDA inspection document on file for HK INNO.N CORPORATION is a Form 483 dated Jan 24, 2025, for the site in Heungbeok Cheongju, South Korea.
What did FDA cite at HK INNO.N CORPORATION?
The regulations cited most in the observations on file for HK INNO.N CORPORATION are 21 CFR 211.113 (Control of microbiological contamination), 2 times; 21 CFR 211.22 (Responsibilities of quality control unit), 2 times; 21 CFR 211.122 (Materials examination and usage criteria), 1 time.