FDA inspection

QualTech Laboratories, Inc.: FDA inspection ending Jan 11, 2018

FDA inspection 1040300 · No Action Indicated (NAI) · Ocean, NJ

Key facts

Inspection ID 1040300
Firm QualTech Laboratories, Inc.
FEI number 3000209713
Address 104 Green Grove Rd
City Ocean
State NJ
ZIP 07712
Country United States
Fiscal year 2018
Inspection end date Jan 11, 2018
Classification No Action Indicated (NAI)
Project area Monitoring of Marketed Animal Drugs, Feed, and Devices
Product type Veterinary

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 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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