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ShangRao Chunyu Technology CO.,LTD. FDA Inspection Record

FEI 3015958566 · Inspections, Form 483s, warning letters and import refusals

ShangRao Chunyu Technology CO.,LTD. is an FDA-registered facility (FEI 3015958566) located in Shangrao, CN. Registered operations: MANUFACTURE.

What FDA found at this site

Inspections on record
None in FDA's published inspection data
Warning letters
1 listed by FDA for this FEI, latest Feb 3, 2021
Import refusals
10 or more

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.

Warning letters

Letters whose text states this FEI. Many letters do not state one, so this list can be incomplete: search warning letters by company name.

FDA record score

Not scored. FDA's published inspection data has no inspection for this site, and the score is only counted for inspected sites. This is not a score of 0. The records FDA does list for this FEI are below.

Counted on Nov 15, 2026, method version 1. How this is counted.

1 record FDA lists for this FEI
RecordDatePoints x age weightAdds
Warning letter, no close-out letter listedFeb 3, 2021The site is not scored, so it adds no points0

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 15, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 15, 2026Newest record Nov 5, 2026Current
Compliance actions (warning letters, injunctions and other action types)Nov 2, 2026Newest record Oct 29, 2026Current
Warning letter textNov 14, 2026Newest record Nov 10, 2026Current
Recalls (Enforcement Report)Nov 15, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 2, 2026Newest record Oct 22, 2026Current

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Facility details

Location
Shangrao (CN)
Registration Expires
Dec 31, 2026
Operations
MANUFACTURE
Source
decrs

Compliance actions

Import refusals

FDA data resources

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