FDA Inspection 1267900 — Pedia Parents Inc.

Pedia Parents Inc. — FEI 1000122497

The FDA completed an inspection of Pedia Parents Inc. on Apr 24, 2025 in Buffalo, 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
Apr 24, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Buffalo, NY (United States)

Citations

IDCFRDescription
260421 CFR 820.30(e)Design review - Lack of or inadequate procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
366621 CFR 820.20(c)Management review - Lack of or inadequate procedures

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