FDA Inspection 672669 — TheraCom

TheraCom — FEI 3008287922

The FDA completed an inspection of TheraCom on Jul 22, 2010 in Rockville, MD. 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
Jul 22, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Rockville, MD (United States)

Additional Details

Risk Evaluation and Mitigation Strategies (REMS)