FDA Inspection 1112521 — Maguire Enterprises, Inc.

Maguire Enterprises, Inc. — FEI 1049754

The FDA completed an inspection of Maguire Enterprises, Inc. on December 11, 2019 in Sunrise, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 9 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 11, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sunrise, FL (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
232721 CFR 820.22Quality audits - Lack of or inadequate procedures
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
334521 CFR 820.200(a)Servicing - Lack of or inadequate procedures
366621 CFR 820.20(c)Management review - Lack of or inadequate procedures
368021 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
369621 CFR 820.100(b)Documentation
421221 CFR 806.20(b)(4)Justification for not reporting
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures