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Manufacturing facility

Mipharm Spa

A single plant registered with the FDA to make drugs for the US market. Below is where it is and the drugs whose FDA labels list this site as performing a manufacturing step — so if this plant has a problem, these are the products that could be affected.

Country
Italy
Registered address
VIA BERNARDO QUARANTA 12, MILANO, 20141, Italy (ITA)
Operations here
analysislabelmanufacturepack
FDA identifiers
FEI 3002807647 · DUNS 514042399

FDA inspection history

Outcomes of closed FDA inspections at this site (drug and biologic program areas).

  • VAIDrug Quality Assurance2024-02-29
  • VAIDrug Quality Assurance2023-09-22
  • VAIDrug Quality Assurance2019-10-17
  • VAIDrug Quality Assurance2017-02-03
  • VAIDrug Quality Assurance2014-02-14
  • VAIDrug Quality Assurance2013-09-27
  • NAIDrug Quality Assurance2011-06-10

Drugs this plant is listed as making

6 distinct drugs across 6 products name this site in their FDA label.

Sources:the establishment's name, address, and country from FDA's Drug Establishments Current Registration Site (DECRS); the drug-to-facility links from DailyMed SPL drug labels, matched by the facility's DUNS number; inspection outcomes from the FDA Data Dashboard, matched by FEI; shortage status from FDA's drug shortage database. More on how this is built. Educational only.