FDA inspection

CellEra LLC: FDA inspection ending Apr 14, 2022

FDA inspection 1167025 · Voluntary Action Indicated (VAI) · Monroe, OH

Key facts

Inspection ID 1167025
Firm CellEra LLC
FEI number 3007594734
Address 1045 Reed Dr Ste C
City Monroe
State OH
ZIP 45050
Country United States
Fiscal year 2022
Inspection end date Apr 14, 2022
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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