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Manufacturing facility

Mikart, LLC

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
2090 Marietta Boulevard NW, Atlanta, Georgia (GA) 30318, United States (USA)
Operations here
manufacture
FDA identifiers
FEI 1050658 · DUNS 013322387

FDA inspection history

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

  • NAIDrug Quality Assurance2022-04-26
  • NAIBioresearch Monitoring2021-09-08
  • VAIDrug Quality Assurance2019-01-18
  • NAIBioresearch Monitoring2018-08-23
  • NAIDrug Quality Assurance2017-11-16
  • NAIDrug Quality Assurance2016-05-03
  • VAIDrug Quality Assurance2014-04-23
  • VAIDrug Quality Assurance2011-08-05
  • NAIDrug Quality Assurance2011-01-20
  • NAIDrug Quality Assurance2010-11-12
  • VAIBioresearch Monitoring2010-09-29
  • NAIDrug Quality Assurance2010-06-16
  • VAIDrug Quality Assurance2009-03-09
  • VAIPostmarket Surv. and Epidemiology2009-03-09

Drugs this plant is listed as making

2 distinct drugs across 5 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.