Suppliers / Chemport

Chemport

South Korea Updated 9 July 2026

Chemport is an API manufacturer based in South Korea. It holds one active US drug master file. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 14 December 2023 as NAI.

1
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
3 of 3 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 14 December 2023 NAI US FDA
  • 11 December 2015 NAI US FDA
  • 11 April 2013 NAI US FDA

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

Registered plants

Site FDA FEI
South, South Korea 3008221008

What they file, and where

Molecule Regulators Docs
Omega-3-Acid Ethyl Esters US FDA 1

Also appears on these molecule pages

Omega-3-Acid Ethyl Esters API

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA None 1

Questions about Chemport

Does Chemport hold a US DMF or a CEP?
Chemport holds 1 active US drug master file. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Is Chemport FDA-registered?
One site operated by Chemport 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 Chemport's last inspection go?
The most recent inspection on record closed on 14 December 2023 as NAI (No Action Indicated: nothing objectionable was found). 3 inspections are on file.
Where does Chemport manufacture?
1 registered site is on record, in South Korea (South). Every site is listed on this page with the register it came from.
What does Chemport make?
1 molecule is on record against Chemport, including Omega-3-Acid Ethyl Esters. Each links through to that molecule's full manufacturer list.
Which regulators recognise Chemport's GMP?
Current GMP certificates are on record from US FDA. GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

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 NAI, on 14 December 2023.

Comparable suppliers

KinOmega Biopharm shares 1 molecule Shandong Yuwang Pharmaceutical shares 1 molecule Croda International shares 1 molecule

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates