FDA Inspection
Steritec Products Mfg. Co., Inc.Steritec Products Mfg. Co., Inc. – FDA Inspection, Jun 2, 2009
Record Details
This FDA Inspection record concerns Steritec Products Mfg. Co., Inc., with an inspection on June 2, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- June 2, 2009
- Product Type
- Devices
View Company Profile
ID · 11ef6a7c-7584-4983-a204-2989923398b6
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 585881
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: 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 |
| August 12, 2010 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: 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 675641 - 2010-08-12
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