FDA Inspection 1034385 — DDSGadget, Inc

DDSGadget, Inc — FEI 3013550004

The FDA completed an inspection of DDSGadget, Inc on Dec 6, 2017 in Bridgeton, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Dec 6, 2017
Fiscal Year
2018
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Bridgeton, MO (United States)

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