Source: FDA, document on fileFDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it.
To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3004610520.
Loop Plaza Pharmacy Company DBA Loop Compounding Pharmacy
Saint Albans, West Virginia, United States
Issue DateJanuary 09, 2017
FEI Number3004610520
CountryUnited States
Status
No Warning Letter
Product Type
Drugs
Establishment Type
Producer of Sterile Drug Products
Sub Systems Impacted
7
Area CleaningContamination ControlDrug Product Containers & ClosuresEnvironmental MonitoringInvestigationsSample TestingStability Studies
Quality Systems
Quality SystemFacilities & EquipmentLaboratory ControlsProduction SystemMaterials System
Loop Plaza Pharmacy Company DBA Loop Compounding Pharmacy FDA Form 483, Saint Albans, West Virginia, January 9, 2017
