Embolx, Inc.

Form 483FOIA Uncovered

Sunnyvale, California, United StatesFEI 3011660785Issued January 19, 2023

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3011660785.

Observations6

Issue DateJanuary 19, 2023

StatusNo Warning Letter

Related Inspections2

Establishment Details

Firm: Embolx, Inc.
Location: Sunnyvale, California, United States
FEI Number: 3011660785
Product Type: Devices
Issue Date: January 19, 2023
Country: United States

Inspection History, 2019 to 2023

NAI1

VAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

Act on This Form 483

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Embolx, Inc. FDA Form 483, Sunnyvale, California, January 19, 2023