FDA Inspection 1334004 — Nutek Bravo, LLC.

Nutek Bravo, LLC. — FEI 3015542130

The FDA completed an inspection of Nutek Bravo, LLC. on Aug 25, 2026 in Hayward, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 25, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Hayward, CA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.