FDA inspection

Persyst Development Corp: FDA inspection ending May 19, 2017

FDA inspection 1023508 · No Action Indicated (NAI) · Solana Beach, CA

Key facts

Inspection ID 1023508
Firm Persyst Development Corp
FEI number 3002624053
Address 3177 Clearwater Dr
City Solana Beach
State CA
ZIP 92075
Country United States
Fiscal year 2017
Inspection end date May 19, 2017
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

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