FDA record · 503B outsourcing facility

Turbare Manufacturing: FDA 503B outsourcing facility record

Turbare Manufacturing in Conway, AR is on FDA's register of 503B outsourcing facilities. Registered since Jun 23, 2023; last FDA inspection May 7, 2026; Form 483 issued at that inspection: Yes; action FDA lists: Open. Register updated by FDA Sep 30, 2026.

Julian CaraulaniFounder, PriceTracker GLP-1FDA register read Oct 3

Status: Registered since Jun 23, 2023; last FDA inspection May 7, 2026.

What FDA’s register states

FDA register entry for Turbare Manufacturing
Field	What FDA’s record states	Source
Facility	Turbare Manufacturing	FDA register
Location	Conway, AR	FDA register
First registered	Jun 23, 2023	FDA register
Most recent registration	Dec 3, 2025	FDA register
Last FDA inspection	May 7, 2026	FDA register
Form 483 issued	Yes	FDA register
Recall conducted	Not published by FDA	FDA register
Action based on last inspection	Open	FDA register
Earlier compounding action	FDA notes at least one previous compounding inspection that resulted in a Form 483, warning letter or other action	FDA register
Intends to compound sterile drugs from bulk	Yes	FDA register

Registration is a filing, not an approval.A Form FDA 483 lists what investigators observed; in FDA’s words it “does not constitute a final agency determination of whether any condition is in violation of the FD&C Act or any relevant regulations.” “Open” means FDA has not determined whether further action will be taken.

Source

Copied from FDA’s Registered Outsourcing Facilities table ↗, updated by FDA Sep 30, 2026, read Oct 3, 2026. The table does not include State Board of Pharmacy actions. All 98 registered facilities