FDA inspection

Nutek Bravo, LLC.: FDA inspection ending Jul 22, 2021

FDA inspection 1147798 · No Action Indicated (NAI) · Hayward, CA

Key facts

Inspection ID 1147798
Firm Nutek Bravo, LLC.
FEI number 3015542130
Address 26545 Corporate Ave
City Hayward
State CA
ZIP 94545
Country United States
Fiscal year 2021
Inspection end date Jul 22, 2021
Classification No Action Indicated (NAI)
Project area Human Cellular, Tissue, and Gene Therapies
Product type Biologics

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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