# Moss Tubes Inc. – FDA 483, Jul 23, 2026

Source: https://www.keypedia.com/records/483/moss-tubes-inc/0cf2e8a7-8796-4572-9247-807cd7be6dd3

> FDA 483 for Moss Tubes Inc. on July 23, 2026. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Moss Tubes Inc.
- Inspection Date: 2026-07-23
- Product Type: device
- Office Name: Division of Human and Animal Food Operations - East I
- Summary: An FDA inspection of Moss Tubes Inc., a medical device manufacturer in Castleton On Hudson, NY, revealed significant deficiencies in their quality system. The firm failed to adequately document procedures for production, risk management, and complaint handling. These issues indicate a lack of control over critical manufacturing processes and post-market surveillance.

## Related Documents

- [483 - 2021-08-13](https://www.keypedia.com/records/483/moss-tubes-inc/946b3ee8-56b0-4d64-82e4-c345e522201f) — date: August 13, 2021

## Related Officers

- [Matthew D. Schnittker](https://www.keypedia.com/people/matthew-d-schnittker/cf76f07f-db6d-47a0-8412-7eb084d4fe8b)

Company: https://www.keypedia.com/companies/moss-tubes-inc/a89a34fc-3799-4988-90a3-ff6edf0c4fde

Office: https://www.keypedia.com/offices/division-of-human-and-animal-food-operations-east-i/a807f00e-d780-40b8-b233-1eb92ece8961