FDA inspection

InVitroCare, Inc: FDA inspection ending Sep 25, 2012

FDA inspection 800358 · Voluntary Action Indicated (VAI) · Frederick, MD

Key facts

Inspection ID 800358
Firm InVitroCare, Inc
FEI number 3004882774
Address 8415 Progress Dr Unit F
City Frederick
State MD
ZIP 21701
Country United States
Fiscal year 2012
Inspection end date Sep 25, 2012
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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