FDA Inspection
Kenlor Industries, Inc.Kenlor Industries, Inc. – FDA Inspection, Jun 2, 2017
Record Details
This FDA Inspection record concerns Kenlor Industries, Inc., with an inspection on June 2, 2017, issued by the Los Angeles District Office, covering medical devices & rad health.
- Person
- CNTRMMNTR MAGEET (Issuing Officer)
View Company Profile
ID · b41d7926-b05a-4ece-ba00-3e5371962646
Inspection Facts
- Inspection number
- 1021555
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Kenlor Industries, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| September 21, 2020 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 3, 2019 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Kenlor Industries, Inc.
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.