Overview
- 5 FDA inspections are on record.
- 5 inspections produced a Form 483.
- The most recent recorded inspection date is 2025-03-07.
At a glance
Inspections
5
Form 483s
5
EIRs
0
Last outcome
Form 483
Inspection history
FDA inspections on record, most recent first.
| Inspection | Category | Outcome | Form 483 |
|---|---|---|---|
| 3 Mar 2025 – 7 Mar 2025 | Human Drugs | 483 | On file |
| 18 Nov 2019 – 22 Nov 2019 | Human Drugs | 483 | View 483 → |
| 12 Jul 2016 – 15 Jul 2016 | Human Drugs | 483 | On file |
| 10 Mar 2014 – 14 Mar 2014 | Human Drugs | 483 | On file |
| 9 Sep 2010 | Not recorded | 483 | On file |
Observations on record
Form 483 observations cited at this site, most recent first.
22 Nov 2019
21 CFR 211.110(a)
Control procedures to monitor and validate performance
Cited by Santos E Camara
22 Nov 2019
21 CFR 211.22(a)
Authority lacking to review records, investigate errors
Cited by Santos E Camara
Investigators
FDA investigators tied to this site in the record.
Gavin T Cua1 insp.
Crystal Monroy1 insp.
Santos E Camara1 insp.
Kellia N Hicks1 insp.
Jose E Melendez1 insp.
Kristy A Zielny1 insp.
Recurring citations
CFR citation patterns observed across this site's inspections.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 211.100(a) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 211.110(a) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 211.142(b) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 211.22(a) | Cited across public-safe Form 483 observations | 1x |
Full site report
Get the verbatim findings behind Zhejiang Cheng Yi Pharmaceutical Co., Ltd's 5 Form 483s
Source PDFs and recurring CFR citations, so your team knows what this site gets cited for.
- The site's full inspection history, with every Form 483 and its outcome
- Warning letters and recalls tied to the company behind it
- Whether recurring CFR citations get closed out or repeat