Changzhou Maokang Medical Products Co., Ltd
FDA inspection history in Changzhou, China, 2018
- 1
- Form 483
Every document, by year
- Form 483
2018: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at Changzhou, China.
Cited most
Across all Changzhou Maokang Medical Products Co. observations on file
- 21 CFR 211.160General requirements1
- 21 CFR 211.165Testing and release for distribution1
- 21 CFR 211.194Laboratory records1
The complete Changzhou Maokang Medical Products Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Changzhou, China
One Form 483 · 2018 · 2 observations
Latest: Form 483, Aug 24, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-08-24 | 483 Form 483 | Changzhou, China | 2 | $99 |
Investigators on these documents
FEI number 3010623099 · most recent document Aug 24, 2018
About Changzhou Maokang Medical Products Co., Ltd
How many FDA Form 483s has Changzhou Maokang Medical Products Co., Ltd received?
FDA Intel has 1 Form 483 on file for Changzhou Maokang Medical Products Co., Ltd; the most recent is dated Aug 24, 2018.
When was Changzhou Maokang Medical Products Co., Ltd last inspected by FDA?
The most recent FDA inspection document on file for Changzhou Maokang Medical Products Co., Ltd is a Form 483 dated Aug 24, 2018, for the site in Changzhou, China.
What did FDA cite at Changzhou Maokang Medical Products Co., Ltd?
The regulations cited most in the observations on file for Changzhou Maokang Medical Products Co., Ltd are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.165 (Testing and release for distribution), 1 time; 21 CFR 211.194 (Laboratory records), 1 time.