FDA Inspection 1282008 — Herbert Ho Loong

Herbert Ho Loong — FEI 3038192500

The FDA completed an inspection of Herbert Ho Loong on Aug 22, 2025 in Shatin, N.T., HKSAR. 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
Aug 22, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Shatin, N.T., HKSAR (Hong Kong SAR)

Additional Details

Clinical Investigator (CI)

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