FDA Inspection 1053259 — GVS TM, Inc

GVS TM, Inc — FEI 2013342

The FDA completed an inspection of GVS TM, Inc on May 15, 2018 in Covina, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 15, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Covina, CA (United States)

Citations

IDCFRDescription
126321 CFR 211.68(b)Computer control of master formula records
203121 CFR 211.194(a)Complete test data included in records

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.