FDA inspection

Cellestis Inc: FDA inspection ending Mar 25, 2015

FDA inspection 918357 · Official Action Indicated (OAI) · Santa Clarita, CA

Key facts

Inspection ID 918357
Firm Cellestis Inc
FEI number 3003964343
Address 28358 Constellation Rd Ste 698
City Santa Clarita
State CA
ZIP 91355
Country United States
Fiscal year 2015
Inspection end date Mar 25, 2015
Classification Official Action Indicated (OAI)
Project area Compliance: Devices
Product type Devices
Warning letter 458031

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • Yes Warning letter followed
  • Yes 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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