FDA-Inspected Site

Zhejiang Lepu Pharmaceutical Co., Ltd.

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

483· Form 483 issued

Taizhou, China · Last updated August 15, 2026

Overview

  • 5 FDA inspections are on record.
  • 2 inspections produced a Form 483.
  • The most recent recorded inspection date is 2025-04-25.

At a glance

Inspections

5

Form 483s

2

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
21 Apr 2025 – 25 Apr 2025Human Drugs483On file
3 Dec 2018 – 7 Dec 2018Human Drugs483On file
25 Aug 2014 – 29 Aug 2014Human DrugsClean
15 Apr 2011Not recordedClean
3 Feb 2008Not recordedClean

Investigators

FDA investigators tied to this site in the record.

Full site report

Get the verbatim findings behind Zhejiang Lepu Pharmaceutical Co., Ltd.'s 2 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