FDA Inspection 1056474 — Tetraphase Pharmaceuticals, Inc.

Tetraphase Pharmaceuticals, Inc. — FEI 3006709821

The FDA completed an inspection of Tetraphase Pharmaceuticals, Inc. on Jun 8, 2018 in Watertown, MA. 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 8, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Watertown, MA (United States)

Additional Details

Sponsor, Contract Research Organization