FDA Inspection 694963 — Helena Laboratories, Corp.
The FDA completed an inspection of Helena Laboratories, Corp. on October 29, 2010 in Beaumont, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- October 29, 2010
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Beaumont, TX (United States)