FDA Inspection 654393 — Syntermed, Inc.

Syntermed, Inc. — FEI 3003079232

The FDA completed an inspection of Syntermed, Inc. on Mar 22, 2010 in Atlanta, GA. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 22, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Atlanta, GA (United States)

Citations

IDCFRDescription
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures