FDA Inspection 663115 — Stegman Laboratories, LLC

Stegman Laboratories, LLC — FEI 3004953984

The FDA completed an inspection of Stegman Laboratories, LLC on May 19, 2010 in Phoenix, AZ. 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). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 19, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Phoenix, AZ (United States)