FDA inspection

Mibo Medical Group: FDA inspection ending Sep 30, 2019

FDA inspection 1105940 · No Action Indicated (NAI) · Dallas, TX

Key facts

Inspection ID 1105940
Firm Mibo Medical Group
FEI number 3011407851
Address 2526 Manana Dr Ste 105
City Dallas
State TX
ZIP 75220
Country United States
Fiscal year 2019
Inspection end date Sep 30, 2019
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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