Changzhou Sunlight Pharmaceutical Co. Ltd.
FDA inspection history in Changzhou, China, 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 Changzhou, China.
Cited most
Across all Changzhou Sunlight Pharmaceutical Co. observations on file
- 21 CFR 211.100Written procedures; deviations1
The complete Changzhou Sunlight Pharmaceutical Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Changzhou, China
One Form 483 · 2024 · 1 observation
Latest: Form 483, May 31, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-05-31 | 483 Form 483 | Changzhou, China | 1 | $99 |
Investigators on these documents
FEI number 3003662818 · most recent document May 31, 2024
About Changzhou Sunlight Pharmaceutical Co. Ltd.
How many FDA Form 483s has Changzhou Sunlight Pharmaceutical Co. Ltd. received?
FDA Intel has 1 Form 483 on file for Changzhou Sunlight Pharmaceutical Co. Ltd.; the most recent is dated May 31, 2024.
When was Changzhou Sunlight Pharmaceutical Co. Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Changzhou Sunlight Pharmaceutical Co. Ltd. is a Form 483 dated May 31, 2024, for the site in Changzhou, China.
What did FDA cite at Changzhou Sunlight Pharmaceutical Co. Ltd.?
The regulations cited most in the observations on file for Changzhou Sunlight Pharmaceutical Co. Ltd. are 21 CFR 211.100 (Written procedures; deviations), 1 time.