FDA Inspection 1276546 — Pedicraft, Inc.

Pedicraft, Inc. — FEI 1043568

The FDA completed an inspection of Pedicraft, Inc. on July 25, 2025 in Jacksonville, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 25, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Jacksonville, FL (United States)

Citations

IDCFRDescription
232821 CFR 820.22Quality audits - auditor independence
313021 CFR 820.100(a)Lack of or inadequate procedures