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FDA Inspection 731969 — Pedicraft, Inc.

Pedicraft, Inc. — FEI 1043568

The FDA completed an inspection of Pedicraft, Inc. on June 28, 2011 in Jacksonville, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 28, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Jacksonville, FL (United States)

Facility

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