FDA Inspection 1048412 — Nusmile, Ltd.

Nusmile, Ltd. — FEI 3006444232

The FDA completed an inspection of Nusmile, Ltd. on Apr 16, 2018 in Houston, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 9 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 16, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Houston, TX (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
311821 CFR 820.75(a)Documentation
312021 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities
322621 CFR 820.70(g)(1)Maintenance schedule, Lack of or inadequate schedule
326421 CFR 820.250(b)Sampling methods - Lack of or inadequate procedures
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
343321 CFR 820.75(c)Process changes - review, evaluation and revalidation
368021 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
369621 CFR 820.100(b)Documentation