Robert C. G. Martin, II, M.D., PhD.

Form 483

Louisville, Kentucky, United StatesFEI 3005063230Issued January 25, 2017

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 3005063230.

Observations2

Issue DateJanuary 25, 2017

StatusNo Warning Letter

Related Inspections2

Establishment Details

Firm: Robert C. G. Martin, II, M.D., PhD.
Location: Louisville, Kentucky, United States
FEI Number: 3005063230
Product Type: Devices
Issue Date: January 25, 2017
Country: United States

Inspection History, 2010 to 2017

NAI1

VAI1

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

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Robert C. G. Martin, II, M.D., PhD. FDA Form 483, Louisville, Kentucky, January 25, 2017