FDA Inspection
Gingi-Pak A Division of the Belport Co., IncGingi-Pak A Division of the Belport Co., Inc – FDA Inspection, Mar 14, 2012
Record Details
This FDA Inspection record concerns Gingi-Pak A Division of the Belport Co., Inc, with an inspection on March 14, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- March 14, 2012
- Product Type
- Devices
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ID · b0fd05aa-4692-4ed6-b020-1089e61113b2
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 775564
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Gingi-Pak A Division of the Belport Co., Inc
4| Date | Classification | Office | Project area |
|---|---|---|---|
| November 12, 2021 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 23, 2019 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 9, 2017 | Not classified | Los Angeles District Office | Drug Quality Assurance |
| September 30, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Gingi-Pak A Division of the Belport Co., Inc
- FDA Inspection 1156779 - 2021-11-12
- FDA Inspection 1082109 - 2019-01-23
- FDA Inspection 1013526 - 2017-06-09
- FDA Inspection 896678 - 2014-09-30
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