FDA Inspection 930309 — Laser Biotech International, Inc.

Laser Biotech International, Inc. — FEI 3004769071

The FDA completed an inspection of Laser Biotech International, Inc. on Jun 19, 2015 in North Chesterfield, VA. 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
Jun 19, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
North Chesterfield, VA (United States)

Citations

IDCFRDescription
520821 CFR 1040.11(a)(2)Calibration of measurement system

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.