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Zhejiang Chemsyn Pharm Co.Ltd FDA Inspection Record

FEI 3011868598 · Inspections, Form 483s, warning letters and import refusals

Zhejiang Chemsyn Pharm Co.Ltd is an FDA-registered facility (FEI 3011868598) located in Zhejiang, CN. Registered operations: API MANUFACTURE. RegDataLab tracks 1 FDA inspection at this facility.

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What FDA found at this site

Latest inspection
May 1, 2025: No Action Indicated (NAI)
Inspections on record
1 (1 NAI)
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

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
May 1, 2025No Action Indicated (NAI)No citations listed

Facility details

Company
Zhejiang Chemsyn Pharm Co., Ltd.
Location
Zhejiang (CN)
Registration Expires
Dec 31, 2026
Operations
API MANUFACTURE
Source
decrs

FDA data resources

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