Manish Mehta, MD

Form 483

Albany, New York, United StatesFEI 3009579540Issued June 13, 2012

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 3009579540.

Observations1

Issue DateJune 13, 2012

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Manish Mehta, MD
Location: Albany, New York, United States
FEI Number: 3009579540
Product Type: Devices
Issue Date: June 13, 2012
Country: United States

Inspection History, 2011 to 2015

NAI2

VAI1

OAI1

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

Act on This Form 483

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Manish Mehta, MD FDA Form 483, Albany, New York, June 13, 2012