FDA Inspection 782065 — Pedia Parents Inc.

Pedia Parents Inc. — FEI 1000122497

The FDA completed an inspection of Pedia Parents Inc. on April 25, 2012 in Buffalo, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 25, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Buffalo, NY (United States)