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Manufacturing facility

L. Perrigo Company

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
United States
Registered address
515 Eastern Ave, Allegan, Michigan (MI) 49010, United States (USA)
Operations here
analysislabelmanufacturepackrepack
FDA identifiers
FEI 1811666 · DUNS 006013346

FDA inspection history

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

  • VAIBioresearch Monitoring2026-02-20
  • VAIDrug Quality Assurance2025-03-19
  • NAIBioresearch Monitoring2023-10-06
  • VAIDrug Quality Assurance2019-01-17
  • NAIBioresearch Monitoring2014-12-11
  • VAIDrug Quality Assurance2014-09-04
  • VAIDrug Quality Assurance2013-11-07
  • NAIDrug Quality Assurance2013-05-17
  • VAIDrug Quality Assurance2012-07-10
  • NAIUnapproved and Misbranded Drugs2012-06-07
  • NAIBioresearch Monitoring2012-05-08
  • VAIDrug Quality Assurance2012-05-08
  • VAIDrug Quality Assurance2011-03-21
  • NAIDrug Quality Assurance2011-03-09
  • NAIDrug Quality Assurance2010-06-28
  • NAIDrug Quality Assurance2010-03-17
  • VAIDrug Quality Assurance2010-02-11
  • OAIDrug Quality Assurance2010-01-14
  • VAIPostmarket Surv. and Epidemiology2009-01-27
  • NAIBioresearch Monitoring2009-01-16
  • VAIDrug Quality Assurance2008-11-07

Drugs this plant is listed as making

1 distinct drugs across 1 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.