FDA inspection

Acro Biotech Inc.: FDA inspection ending Sep 3, 2013

FDA inspection 850016 · No Action Indicated (NAI) · Rancho Cucamonga, CA

Key facts

Inspection ID 850016
Firm Acro Biotech Inc.
FEI number 3005670738
Address 9500 7th St Ste M
City Rancho Cucamonga
State CA
ZIP 91730
Country United States
Fiscal year 2013
Inspection end date Sep 3, 2013
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

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

Browse all FDA inspections