FDA Inspection
Steritec Products Mfg. Co., Inc.Steritec Products Mfg. Co., Inc. – FDA Inspection, May 1, 2013
Record Details
This FDA Inspection record concerns Steritec Products Mfg. Co., Inc., with an inspection on May 1, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- May 1, 2013
- Product Type
- Devices
View Company Profile
ID · fa054a24-804c-4708-8b8e-8b1c5e809ef7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 831157
- 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 |
| August 12, 2010 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: 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 675641 - 2010-08-12
- FDA Inspection 585881 - 2009-06-02
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