FDA Inspection 838587 — Dr. Joel Kaplan, Inc.

Dr. Joel Kaplan, Inc. — FEI 3001890611

The FDA completed an inspection of Dr. Joel Kaplan, Inc. on July 17, 2013 in San Diego, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
July 17, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)

Citations

IDCFRDescription
1471221 CFR 820.184DHR - not or inadequately maintained
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures