# Turbare Manufacturing – FDA Inspection, May 7, 2026

Source: https://www.keypedia.com/records/fda_inspections/turbare-manufacturing/0791d146-5976-48e8-aa95-841b58fe4aa8
Source feed: FDA_Inspections

> FDA inspection 1305264 of Turbare Manufacturing, May 07, 2026. 4 citations under 21 CFR part 211. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1305264
- Company Name: Turbare Manufacturing
- Inspection Date: 2026-05-07
- Project Area: Drug Quality Assurance
- Product Type: Human Drugs
- Center: Human Drugs
- Office Name: Dallas District Office
- Citation Count: 4

## Related Documents

- [FDA Inspection 1259059 - 2025-01-24](https://www.keypedia.com/records/fda_inspections/turbare-manufacturing/0d7e9368-37a2-4e5c-8858-61dcd15fa8ab)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/sangeeta-m-khurana/bed4533f-a9aa-47c5-9e0b-f20ad36461aa)

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