FDA Inspection 1329270 — Liquidia Technologies, Inc.

Liquidia Technologies, Inc. — FEI 3008731457

The FDA completed an inspection of Liquidia Technologies, Inc. on Jun 12, 2026 in Morrisville, NC. 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
Jun 12, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Morrisville, NC (United States)

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