# FDA Inspection 1087852 - Viking Rubber Products Inc. - April 29, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/viking-rubber-products-inc/da3a536e-60a7-45e1-9cb7-f2bb115dce4e
Source feed: FDA_Inspections

> FDA Inspection 1087852 for Viking Rubber Products Inc. on April 29, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1087852
- Company Name: Viking Rubber Products Inc.
- Inspection Date: 2019-04-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1230857 - 2024-02-15](https://www.globalkeysolutions.net/records/fda_inspections/viking-rubber-products-inc/5bb6a101-4fd0-4221-b587-062e1e64f939)
- [FDA Inspection 1087852 - 2019-04-29](https://www.globalkeysolutions.net/records/fda_inspections/viking-rubber-products-inc/8c715854-333a-4691-87c3-b1c4ea82a0a8)

Company: https://www.globalkeysolutions.net/companies/viking-rubber-products-inc/45d90f34-30b4-4ff5-a5e5-c7a5feca817c

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7