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Peking Medicine Manufactory FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

Peking Medicine Manufactory has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 2 compliance actions on record. FDA has issued 2 warning letters to Peking Medicine Manufactory, the most recent on Mar 25, 2013.

What these totals cover: FDA records filed under the name "Peking Medicine Manufactory".

Latest inspection: Apr 30, 2012 · OAI

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 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions	2	Nov 2, 2026	Newest record Oct 29, 2026	Current

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Peking Medicine Manufactory FDA Warning Letters

2 warning letters from Apr 5, 2012 to Mar 25, 2013.

Issued	Subject	Issuing office	Close-out letter
Mar 25, 2013 · Record page
Apr 5, 2012 · Record page

A warning letter is FDA's formal notice that a company has violated FDA requirements. Each date links to the letter on fda.gov where FDA has it online. Search the text of every letter with the FDA warning letter search.

Recent FDA inspections

1 inspection on Apr 30, 2012.

Date	Site	Product	Classification	FEI
Apr 30, 2012	Tsuen Wan, Hong Kong SAR	Drugs	Official Action Indicated (OAI)	3004186759

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 2 compliance actions under Peking Medicine Manufactory: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Mar 25, 2013.

The warning letters in this data are listed above, together with the letters FDA posts online; a letter found in both is shown once. Other 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 3004186759	Tsuen Wan, Hong Kong SAR	1	Apr 30, 2012

Peking Medicine Manufactory and the FDA: common questions

Has Peking Medicine Manufactory received an FDA warning letter?

Yes. FDA has issued 2 warning letters to Peking Medicine Manufactory. The most recent is dated Mar 25, 2013.

Has Peking Medicine Manufactory received an FDA Form 483?

FDA has not published a Form 483 for "Peking Medicine Manufactory" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Peking Medicine Manufactory?

The most recent FDA inspection on file ended Apr 30, 2012 at Tsuen Wan, Hong Kong SAR and was classified OAI. FDA has 1 inspection of Peking Medicine Manufactory on file, 1 of them classified OAI (official action indicated).

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