AMO (Hangzhou) Co., Ltd.
FDA inspection history in Hangzhou, China, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Hangzhou, China.
Cited most
Across all AMO (Hangzhou) Co. observations on file
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete AMO (Hangzhou) Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Hangzhou, China
One Form 483 · 2019 · 3 observations
Latest: Form 483, Jul 2, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-07-02 | 483 Form 483 | Hangzhou, China | 3 | $99 |
Investigators on these documents
FEI number 3004178847 · most recent document Jul 2, 2019
About AMO (Hangzhou) Co., Ltd.
How many FDA Form 483s has AMO (Hangzhou) Co., Ltd. received?
FDA Intel has 1 Form 483 on file for AMO (Hangzhou) Co., Ltd.; the most recent is dated Jul 2, 2019.
When was AMO (Hangzhou) Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for AMO (Hangzhou) Co., Ltd. is a Form 483 dated Jul 2, 2019, for the site in Hangzhou, China.
What did FDA cite at AMO (Hangzhou) Co., Ltd.?
The regulations cited most in the observations on file for AMO (Hangzhou) Co., Ltd. are 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.