FDA Inspection 1250892 — LaunchPOrt Llc

LaunchPOrt Llc — FEI 3015259858

The FDA completed an inspection of LaunchPOrt Llc on Sep 11, 2024 in Baltimore, MD. 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
Sep 11, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Baltimore, MD (United States)

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