FDA Inspection 1113302 — Novetide Ltd.

Novetide Ltd. — FEI 3002807897

The FDA completed an inspection of Novetide Ltd. on Nov 14, 2019 in Netanya. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Nov 14, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Netanya (Israel)

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