FDA Inspection 927879 — SWG Labs, Inc.

SWG Labs, Inc. — FEI 3003963141

The FDA completed an inspection of SWG Labs, Inc. on June 2, 2015 in Las Vegas, NV. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 2, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Las Vegas, NV (United States)

Citations

IDCFRDescription
1471021 CFR 820.150Lack of or inadequate procedures for storage.
323221 CFR 820.72(a)Equipment suitability & capability
328521 CFR 820.90(b)(2)Product rework procedures, Lack of or inadequate procedures