FDA inspection

Antarma LLC: FDA inspection ending Sep 23, 2022

FDA inspection 1180138 · Voluntary Action Indicated (VAI) · New York, NY

Key facts

Inspection ID 1180138
Firm Antarma LLC
FEI number 3014117096
Address 276 5th Ave Rm 704
City New York
State NY
ZIP 10001
Country United States
Fiscal year 2022
Inspection end date Sep 23, 2022
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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