Cetro America Inc.

Form 483FOIA Uncovered

Meriden, Connecticut, United StatesFEI 3004167720Issued January 11, 2018

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 3004167720.

Observations1

Issue DateJanuary 11, 2018

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Cetro America Inc.
Location: Meriden, Connecticut, United States
FEI Number: 3004167720
Product Type: Devices
Issue Date: January 11, 2018
Country: United States

Inspection History, 2018 to 2026

NAI1

VAI3

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

Act on This Form 483

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Cetro America Inc. FDA Form 483, Meriden, Connecticut, January 11, 2018