FDA Inspection 1064461 — Pedia Parents Inc.

Pedia Parents Inc. — FEI 1000122497

The FDA completed an inspection of Pedia Parents Inc. on Aug 8, 2018 in Buffalo, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Aug 8, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Buffalo, NY (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.