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.
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
Inspections
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 |
| Germany, Germany | 3002853327 |
| Wahlstedt, Germany | Not on file |
Filings and GMP by regulator
| Regulator | Filings | GMP certificates |
| NPRA (MY) | 2 | None |
| ZLG (DE) | None | 14 |
| EMA | None | 1 |
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Open risk flags
- The most recent inspection outcome was VAI, on 17 February 2022.
Sources on this page
- FDA
- Drug master files, establishment registration, inspection classifications
- EDQM
- Certificates of suitability
- EudraGMDP and national regulators
- GMP certificates