# FDA Inspection 954779 - ARMOR PLAST LTD - December 04, 2015

Source: https://www.keypedia.com/records/fda_inspections/armor-plast-ltd/a71b39f1-9481-4232-8148-6790b0a2bfdd
Source feed: FDA_Inspections

> FDA Inspection 954779 for ARMOR PLAST LTD on December 04, 2015. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 954779
- Company Name: ARMOR PLAST LTD
- Inspection Date: 2015-12-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1304528 - 2026-02-26](https://www.keypedia.com/records/fda_inspections/armor-plast-ltd/cc59ce67-0e39-4159-a62f-d279a0fdbc5f)
- [FDA Inspection 1198686 - 2023-01-19](https://www.keypedia.com/records/fda_inspections/armor-plast-ltd/e113af07-1051-40b6-9ddd-0660770e067f)
- [FDA Inspection 954779 - 2015-12-04](https://www.keypedia.com/records/fda_inspections/armor-plast-ltd/be47db82-d261-4c2f-a695-f80ac5dfb033)

Company: https://www.keypedia.com/companies/armor-plast-ltd/a81a70bc-52ed-431c-9511-042e6b692aba

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