Suppliers / Lgm Pharma

Lgm Pharma

United States 142 employees Updated 9 July 2026

Lgm Pharma is a contract manufacturer based in United States. It appears in 1 regulatory filing across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 28 June 2024 as VAI.

0
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
1
filings across 1 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

  • 28 June 2024 VAI US FDA
  • 8 April 2022 OAI US FDA
  • 4 December 2018 OAI US FDA

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

Registered plants

Site FDA FEI
ERLANGER, United States 3012048333

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 1 1

Questions about Lgm Pharma

Does Lgm Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Lgm Pharma. It does have 1 filing with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Is Lgm Pharma FDA-registered?
One site operated by Lgm Pharma 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 Lgm Pharma's last inspection go?
The most recent inspection on record closed on 28 June 2024 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 3 inspections are on file, of which 2 closed as OAI.
Where does Lgm Pharma manufacture?
1 registered site is on record, in United States (Erlanger). Every site is listed on this page with the register it came from.
Which regulators recognise Lgm Pharma'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 VAI, on 28 June 2024.

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Sources on this page

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