Tetracore, Inc.

Form 483

Rockville, Maryland, United StatesFEI 3003517954Issued May 28, 2009

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 3003517954.

Observations4

Issue DateMay 28, 2009

StatusNo Warning Letter

Related Inspections6

Establishment Details

Firm: Tetracore, Inc.
Location: Rockville, Maryland, United States
FEI Number: 3003517954
Product Type: Devices
Issue Date: May 28, 2009
Country: United States

Inspection History, 2009 to 2024

NAI2

VAI3

OAI1

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

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Tetracore, Inc. FDA Form 483, Rockville, Maryland, May 28, 2009