FDA inspection

Permobil Inc: FDA inspection ending Aug 17, 2021

FDA inspection 1149139 · Voluntary Action Indicated (VAI) · Lebanon, TN

Key facts

Inspection ID 1149139
Firm Permobil Inc
FEI number 1221084
Address 300 Duke Dr
City Lebanon
State TN
ZIP 37090
Country United States
Fiscal year 2021
Inspection end date Aug 17, 2021
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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