# FDA Inspection 1259059 - Turbare Manufacturing - January 24, 2025

Source: https://www.keypedia.com/records/fda_inspections/turbare-manufacturing/0d7e9368-37a2-4e5c-8858-61dcd15fa8ab
Source feed: FDA_Inspections

> FDA Inspection 1259059 for Turbare Manufacturing on January 24, 2025. Classification: Official Action Indicated (OAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1259059
- Company Name: Turbare Manufacturing
- Inspection Date: 2025-01-24
- Classification: Official Action Indicated (OAI)
- Project Area: Drug Quality Assurance
- Product Type: Human Drugs
- Office Name: Dallas District Office

Company: https://www.keypedia.com/companies/turbare-manufacturing/855e49f5-275b-4bc8-b275-482465709969

Office: https://www.keypedia.com/offices/dallas-district-office/2d1ee9ae-c44c-4494-8186-a920a69b98f9