Dr. Joel Kaplan, Inc.

Form 483

San Diego, California, United StatesFEI 3001890611Issued July 17, 2013

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 3001890611.

Observations2

Issue DateJuly 17, 2013

Status1 Related Warning Letter

Related Inspections6

Establishment Details

Firm: Dr. Joel Kaplan, Inc.
Location: San Diego, California, United States
FEI Number: 3001890611
Product Type: Devices
Issue Date: July 17, 2013
Country: United States

Inspection History, 2013 to 2025

NAI2

VAI2

OAI2

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

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Dr. Joel Kaplan, Inc. FDA Form 483, San Diego, California, July 17, 2013