FDA-Inspected Site

Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd.

5 FDA inspections are on record for Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd. in Taizhou, China.

Clean· No action indicated

Taizhou, China · Last updated July 10, 2026

Overview

  • 5 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

5

Form 483s

3

EIRs

1

Last outcome

Clean

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
27 Oct 2025 – 31 Oct 2025Human DrugsClean
16 Sep 2019 – 20 Sep 2019Human Drugs483On file
30 Oct 2017 – 2 Nov 2017Human DrugsClean
4 Jul 2016 – 8 Jul 2016Human Drugs483On file
22 Sep 2014 – 26 Sep 2014Human Drugs483On file

Investigators

FDA investigators tied to this site in the record.

Full site report

Get the verbatim findings behind Zhejiang Hisoar Chuannan Pharmaceutical 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