Suppliers / The United Laboratories (Inner Mongolia)

The United Laboratories (Inner Mongolia)

China Updated 9 July 2026

The United Laboratories (Inner Mongolia) is an API manufacturer based in China. Its most recent recorded inspection, by US FDA, closed on 1 December 2017 as VAI.

0
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 1 December 2017 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
China, China 3010166895

What they file, and where

Molecule Regulators Docs
Amoxicillin SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Questions about The United Laboratories (Inner Mongolia)

Is The United Laboratories (Inner Mongolia) FDA-registered?
One site operated by The United Laboratories (Inner Mongolia) carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did The United Laboratories (Inner Mongolia)'s last inspection go?
The most recent inspection on record closed on 1 December 2017 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 1 inspection is on file.
Where does The United Laboratories (Inner Mongolia) manufacture?
1 registered site is on record, in China (China). Every site is listed on this page with the register it came from.
What does The United Laboratories (Inner Mongolia) make?
1 molecule is on record against The United Laboratories (Inner Mongolia), including Amoxicillin. Each links through to that molecule's full manufacturer list.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Open risk flags

  • The most recent inspection outcome was VAI, on 1 December 2017.

Comparable suppliers

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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability