TTY BIOPHARM COMPANY LIMITED CHUNG--LI FACTORY FDA Inspection Record

FEI 3005054986 · Inspections, Form 483s, warning letters and import refusals

TTY BIOPHARM COMPANY LIMITED CHUNG--LI FACTORY is an FDA-registered facility (FEI 3005054986) located in Taoyuan City, TW. Registered operations: ANALYSIS; LABEL; MANUFACTURE; PACK; STERILIZE. RegDataLab tracks 4 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
May 2, 2025: Voluntary Action Indicated (VAI)
Inspections on record
4 (3 VAI, 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 2, 2025Voluntary Action Indicated (VAI)No citations listed
Nov 16, 2018Voluntary Action Indicated (VAI)No citations listed
Mar 18, 2016Voluntary Action Indicated (VAI)No citations listed
Sep 27, 2013No Action Indicated (NAI)No citations listed

Facility details

Company
TTY BioPharm Company Ltd (Chungli Factory)
Location
Taoyuan City (TW)
Registration Expires
Dec 31, 2026
Operations
ANALYSIS; LABEL; MANUFACTURE; PACK; STERILIZE
Source
decrs

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