FDA Inspection 1105192 — BBS Enterprises

BBS Enterprises — FEI 3009887475

The FDA completed an inspection of BBS Enterprises on September 18, 2019 in Mishawaka, IN. 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
September 18, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Mishawaka, IN (United States)