Fujian Kerui Pharmaceutical Co., Ltd. FDA Inspection Record

FEI 3003657686 · Inspections, Form 483s, warning letters and import refusals

Fujian Kerui Pharmaceutical Co., Ltd. is an FDA-registered facility (FEI 3003657686) located in Fujian, CN. Registered operations: API MANUFACTURE. RegDataLab tracks 4 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Apr 25, 2025: Voluntary Action Indicated (VAI)
Inspections on record
4 (4 VAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name
Import refusals
1

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Apr 25, 2025Voluntary Action Indicated (VAI)No citations listed
Mar 16, 2018Voluntary Action Indicated (VAI)No citations listed
May 29, 2015Voluntary Action Indicated (VAI)No citations listed
Feb 19, 2009Voluntary Action Indicated (VAI)No citations listed

Facility details

Company
Fujian Kerui Pharmaceutical Co., Ltd.
Location
Fujian (CN)
Registration Expires
Dec 31, 2027
Operations
API MANUFACTURE
Source
decrs

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.