FDA Inspection 1030858 — Max Mobility LLC

Max Mobility LLC — FEI 3008370857

The FDA completed an inspection of Max Mobility LLC on November 7, 2017 in Lebanon, TN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 7, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Lebanon, TN (United States)

Citations

IDCFRDescription
367621 CFR 820.30(f)Design verification - documentation