FDA Inspection 1112568 — OcuMetrics, Inc.

OcuMetrics, Inc. — FEI 1000221346

The FDA completed an inspection of OcuMetrics, Inc. on December 12, 2019 in Palo Alto, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 4 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 12, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Palo Alto, CA (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
342721 CFR 820.50(a)(2)Supplier oversight
369621 CFR 820.100(b)Documentation
53921 CFR 820.70(b)Production and Process Change Procedures, lack of or Inad.