HEC Pharm Co. Ltd.
FDA inspection history on file, 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.
Cited most
Across all HEC Pharm Co. observations on file
- 21 CFR 211.160General requirements2
- 21 CFR 211.68Automatic, mechanical, and electronic equipment2
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete HEC Pharm Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-11-21 | 483 Form 483 | — | 5 | $99 |
Investigators on these documents
FEI number 3006259537 · most recent document Nov 21, 2025
About HEC Pharm Co. Ltd.
How many FDA Form 483s has HEC Pharm Co. Ltd. received?
FDA Intel has 1 Form 483 on file for HEC Pharm Co. Ltd.; the most recent is dated Nov 21, 2025.
When was HEC Pharm Co. Ltd. last inspected by FDA?
The most recent FDA inspection document on file for HEC Pharm Co. Ltd. is a Form 483 dated Nov 21, 2025.
What did FDA cite at HEC Pharm Co. Ltd.?
The regulations cited most in the observations on file for HEC Pharm Co. Ltd. are 21 CFR 211.160 (General requirements), 2 times; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 2 times; 21 CFR 211.67 (Equipment cleaning and maintenance), 1 time.