FDA inspection

Marlen Manufacturing & Development Co.: FDA inspection ending May 6, 2026

FDA inspection 1315724 · Voluntary Action Indicated (VAI) · Bedford, OH

Key facts

Inspection ID 1315724
Firm Marlen Manufacturing & Development Co.
FEI number 1520020
Address 5150 Richmond Rd
City Bedford
State OH
ZIP 44146
Country United States
Fiscal year 2026
Inspection end date May 6, 2026
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
  • 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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