Orca1

FDA inspection

Navinta, LLC: FDA inspection ending Jun 29, 2023

FDA inspection 1209856 · Ewing, NJ

Key facts

Inspection ID 1209856
Firm Navinta, LLC
FEI number 3004375014
Address 1499 Lower Ferry Rd
City Ewing
State NJ
ZIP 08618-1414
Fiscal year 2023
Inspection end date Jun 29, 2023
Project area Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices|Generic Drug Evaluation|Postmarket Assurance: Medical Devices
Product type Devices, Drugs

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.

Other inspections at this establishment

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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