Overview
- 6 FDA inspections are on record.
- 3 inspections produced a Form 483.
- The most recent recorded inspection date is 2025-10-31.
At a glance
Inspections
6
Form 483s
3
EIRs
0
Last outcome
Form 483
Inspection history
FDA inspections on record, most recent first.
| Inspection | Category | Outcome | Form 483 |
|---|---|---|---|
| 27 Oct 2025 – 31 Oct 2025 | Human Drugs | 483 | On file |
| 21 Oct 2019 – 23 Oct 2019 | Human Drugs | Clean | |
| 11 Dec 2017 – 15 Dec 2017 | Human Drugs | 483 | On file |
| 28 Jul 2014 – 1 Aug 2014 | Human Drugs | 483 | On file |
| 30 Apr 2010 | Not recorded | Clean | |
| 26 Mar 2009 | Not recorded | Clean |
Investigators
FDA investigators tied to this site in the record.
Lisa R Hilliard1 insp.
Christopher T Middendorf1 insp.
Truong X Nguyen1 insp.
Ivis L Negron Torres1 insp.
Gang Wang1 insp.
Marie F Morin1 insp.
Brenda W Uratani1 insp.
Charles I Ahn1 insp.
Paul L Bellamy1 insp.
Full site report
Get the verbatim findings behind Changzhou Qianhong Biopharma Co., Ltd.'s 3 Form 483s
The full inspection record, as Atlas holds it, 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