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Manufacturing facility

GVS TM, Inc

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
1630 W Industrial Park Street, Covina, California (CA) 91722, United States (USA)
Operations here
labelmanufacture
FDA identifiers
FEI 2013342 · DUNS 119067149

Recent inspection flagged official action

FDA classified an inspection here as OAI (official action indicated) within the last two years — the strongest public warning signal a facility gets. This plant is listed on labels for 3 drugs. A supply problem here can ripple to all of them.

FDA inspection history

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

  • OAIBlood and Blood Products2026-05-01
  • NAIBlood and Blood Products2023-09-22
  • VAIDrug Quality Assurance2019-09-25
  • VAIDrug Quality Assurance2018-05-15
  • NAIDrug Quality Assurance2014-08-19
  • VAIDrug Quality Assurance2012-11-08
  • NAIDrug Quality Assurance2011-03-18
  • NAIBlood and Blood Products2010-06-25
  • VAIDrug Quality Assurance2010-06-25

Drugs this plant is listed as making

3 distinct drugs across 3 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.