FDA Inspection 1009128 — Innolatex Sdn. Bhd.

Innolatex Sdn. Bhd. — FEI 3003117682

The FDA completed an inspection of Innolatex Sdn. Bhd. on Mar 9, 2017 in Port Klang. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Mar 9, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Port Klang (Malaysia)

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