FDA Inspection 1090928 — OraLabs, Incorporated

OraLabs, Incorporated — FEI 3001237145

The FDA completed an inspection of OraLabs, Incorporated on May 28, 2019 in Parker, CO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 28, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Parker, CO (United States)

Citations

IDCFRDescription
237121 CFR 820.30(a)Design control - no procedures
63021 CFR 803.17Lack of Written MDR Procedures