FDA inspection

Rainbow Medical Devices Llc: FDA inspection ending Apr 17, 2017

FDA inspection 1013070 · No Action Indicated (NAI) · Mission Viejo, CA

Key facts

Inspection ID 1013070
Firm Rainbow Medical Devices Llc
FEI number 3010304565
Address 782 Strawberry Flds
City Mission Viejo
State CA
ZIP 92692
Country United States
Fiscal year 2017
Inspection end date Apr 17, 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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