FDA Inspection 939267 — OmniActive Health Technologies

OmniActive Health Technologies — FEI 3011153747

The FDA completed an inspection of OmniActive Health Technologies on Jul 31, 2015 in Supa. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 31, 2015
Fiscal Year
2015
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Supa (India)

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