FDA inspection

ARGONAUT MANUFACTURING SERVICES, INC.: FDA inspection ending Apr 26, 2022

FDA inspection 1170240 · No Action Indicated (NAI) · Carlsbad, CA

Key facts

Inspection ID 1170240
Firm ARGONAUT MANUFACTURING SERVICES, INC.
FEI number 3013508066
Address 2841 Loker Ave E
City Carlsbad
State CA
ZIP 92010
Country United States
Fiscal year 2022
Inspection end date Apr 26, 2022
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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