Suppliers / Flamma

Flamma

Italy 462 employees Updated 9 July 2026

Flamma is an API manufacturer based in Italy. It holds 5 active US drug master files and 5 valid CEPs across a filed portfolio of 6 molecules. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 15 December 2023 as VAI.

5
active US DMFs
5
valid CEPs
7
registered plants 3 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
3 of 3 confirmed
Inspections
8 of 8 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 15 December 2023 VAI US FDA
  • 15 April 2022 VAI US FDA
  • 25 March 2022 VAI US FDA
  • 26 July 2019 VAI US FDA
  • 17 March 2017 VAI US FDA
  • 20 May 2016 VAI US FDA
  • 21 March 2014 VAI US FDA
  • 13 March 2014 NAI US FDA

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

Registered plants

Site FDA FEI
ISSO, Italy Not on file
CHIGNOLO D'ISOLA, Italy Not on file
23892 BULCIAGO, Italy Not on file
Chignolo d'Isola, Italy Not on file
Italy, Italy 3001168779
Italy, Italy 3002806311

1 further sites are on record.

What they file, and where

Molecule Regulators Docs
Minoxidil EDQM, SFDA (Saudi Arabia), US FDA 4
Labetalol EDQM, US FDA 2
Melatonin EDQM, US FDA 2
Valaciclovir EDQM, US FDA 2
Azelaic Acid US FDA 1
Nimesulide EDQM 1

Also appears on these molecule pages

Minoxidil contract manufacturing Valaciclovir API Valacyclovir API

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA None 1

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Open risk flags

  • The most recent inspection outcome was VAI, on 15 December 2023.

Sources on this page

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