FDA Inspection
Lutech Industries IncLutech Industries Inc – FDA Inspection, Jul 17, 2015
Record Details
This FDA Inspection record concerns Lutech Industries Inc, with an inspection on July 17, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Lutech Industries Inc
- Inspection Date
- July 17, 2015
- Product Type
- Devices
View Company Profile
ID · 27f7818a-3b46-4e46-a955-183c712e4046
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 941321
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.25(b)Training records
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Lutech Industries Inc
4| Date | Classification | Office | Project area |
|---|---|---|---|
| March 26, 2025 | NAI | New York District Office | Postmarket Assurance: Medical Devices |
| September 10, 2021 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 12, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 18, 2013 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Lutech Industries Inc
- FDA Inspection 1266521 - 2025-03-26
- FDA Inspection 1154488 - 2021-09-10
- FDA Inspection 1028481 - 2017-10-12
- FDA Inspection 852478 - 2013-10-18
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.