FDA Inspection
OmniLife ScienceOmniLife Science – FDA Inspection, Sep 13, 2017
Record Details
This FDA Inspection record concerns OmniLife Science, with an inspection on September 13, 2017, issued by the Center for Devices and Radiological Health, covering devices.
View Company Profile
ID · da50428d-f169-4058-abb9-f420c7873db6
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1025556
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.20(c)Management review - Lack of or inadequate procedures
- 21 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of OmniLife Science
3| Date | Classification | Office | Project area |
|---|---|---|---|
| April 4, 2022 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 6, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 3, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for OmniLife Science
- FDA Inspection 1166323 - 2022-04-04
- FDA Inspection 810557 - 2012-12-06
- FDA Inspection 713580 - 2011-02-03
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.