FDA Inspection 1029048 — Helena Laboratories, Inc
The FDA completed an inspection of Helena Laboratories, Inc on July 14, 2017 in Beaumont, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- July 14, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Beaumont, TX (United States)