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Ko Da Pharmaceutical Co Ltd

FDA Regulatory Profile

Ko Da Pharmaceutical Co Ltd has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 1 compliance action on record.

What these totals cover: FDA records filed under the name "Ko Da Pharmaceutical Co Ltd" and its spelling variant "Ko Da Pharmaceutical Co".

Latest inspection: May 27, 2015 · OAI

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Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	0	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	1	Nov 13, 2026	Newest record Nov 5, 2026	Current
Compliance actions	1	Nov 2, 2026	Newest record Oct 29, 2026	Current

Recent FDA inspections

1 inspection on May 27, 2015.

Date	Site	Product	Classification	FEI
May 27, 2015	Ping Cheng City, Taiwan	Drugs	Official Action Indicated (OAI)	3001878625

NAI: No objectionable conditions or practices were found during the inspection.
VAI: Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI: Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

Compliance Actions

FDA's compliance actions data lists 1 compliance action under Ko Da Pharmaceutical Co Ltd: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, May 27, 2016.

Individual actions are not listed on this page. Search them with the FDA warning letter search or browse all compliance actions.

FDA-inspected facilities

1 inspected site, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3001878625	Ping Cheng City, Taiwan	1	May 27, 2015

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