FDA Inspection
Ostial CorporationOstial Corporation – FDA Inspection, Jan 6, 2017
Record Details
This FDA Inspection record concerns Ostial Corporation, with an inspection on January 6, 2017, issued by the San Francisco District Office, covering medical devices & rad health.
- Company
- Ostial Corporation
- Inspection Date
- January 6, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 137bd258-321f-4ae4-9e77-34a2a37904a6
Inspection Facts
- Inspection number
- 1006023
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Ostial Corporation
3| Date | Classification | Office | Project area |
|---|---|---|---|
| March 25, 2026 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 12, 2023 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| December 20, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Ostial Corporation
- FDA Inspection 1310218 - 2026-03-25
- FDA Inspection 1195624 - 2023-01-12
- FDA Inspection 811464 - 2012-12-20
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