Suppliers / Lichtenheldt Gmbh Pharmazeutische Fabrik

Lichtenheldt Gmbh Pharmazeutische Fabrik

Germany 3 employees Updated 9 July 2026

Lichtenheldt Gmbh Pharmazeutische Fabrik is a finished-dose manufacturer based in Germany. It appears in 2 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by ZLG (DE) and EMA. Its most recent recorded inspection, by US FDA, closed on 17 February 2022 as VAI.

0
active US DMFs
0
valid CEPs
3
registered plants 1 with an FDA FEI number
2
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
1 of 1 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Inspection history

  • 17 February 2022 VAI US FDA

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

Registered plants

Site FDA FEI
Schleswig-Holstein, Germany Not on file
Wahlstedt, Germany Not on file
Germany, Germany 3002853327

Filings and GMP by regulator

Regulator Filings GMP certificates
NPRA (MY) 2 None
ZLG (DE) None 14
EMA None 1

Questions about Lichtenheldt Gmbh Pharmazeutische Fabrik

Does Lichtenheldt Gmbh Pharmazeutische Fabrik hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Lichtenheldt Gmbh Pharmazeutische Fabrik. It does have 2 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Is Lichtenheldt Gmbh Pharmazeutische Fabrik FDA-registered?
One site operated by Lichtenheldt Gmbh Pharmazeutische Fabrik 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 Lichtenheldt Gmbh Pharmazeutische Fabrik's last inspection go?
The most recent inspection on record closed on 17 February 2022 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 1 inspection is on file.
Where does Lichtenheldt Gmbh Pharmazeutische Fabrik manufacture?
3 registered sites are on record, in Germany (Schleswig-holstein, Wahlstedt and Germany). Every site is listed on this page with the register it came from.
Which regulators recognise Lichtenheldt Gmbh Pharmazeutische Fabrik's GMP?
Current GMP certificates are on record from ZLG (DE) and EMA. 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 17 February 2022.

Comparable suppliers

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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