FDA Inspection 544243 — Endo-Therapeutics, Inc.

Endo-Therapeutics, Inc. — FEI 1000132436

The FDA completed an inspection of Endo-Therapeutics, Inc. on Oct 22, 2008 in Clearwater, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 22, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Clearwater, FL (United States)

Citations

IDCFRDescription
48621 CFR 820.50(a)Evaluation of suppliers, contractors, etc., requirements
54621 CFR 820.75(a)Lack of or inadequate process validation