FDA Inspection
Steritec Products Mfg. Co., Inc.Steritec Products Mfg. Co., Inc. – FDA Inspection, Aug 12, 2010
Record Details
This FDA Inspection record concerns Steritec Products Mfg. Co., Inc., with an inspection on August 12, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- August 12, 2010
- Product Type
- Devices
View Company Profile
ID · 1d170122-357b-4f44-ba2d-ff132ae18cf7
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 675641
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Steritec Products Mfg. Co., Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| December 1, 2022 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 1, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 1, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 2, 2009 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Steritec Products Mfg. Co., Inc.
- FDA Inspection 1192098 - 2022-12-01
- FDA Inspection 1000027 - 2017-02-01
- FDA Inspection 831157 - 2013-05-01
- FDA Inspection 585881 - 2009-06-02
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.