FDA Inspection 732614 — Medical Depot Inc.

Medical Depot Inc. — FEI 3002997602

The FDA completed an inspection of Medical Depot Inc. on Jun 17, 2011 in Port Washington, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 17, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Port Washington, NY (United States)

Citations

IDCFRDescription
232721 CFR 820.22Quality audits - Lack of or inadequate procedures
366621 CFR 820.20(c)Management review - Lack of or inadequate procedures
44721 CFR 820.40Lack of procedures, or not maintained