---
title: Dickson Resource Blog | Audits
description: Audits | A blog dedicated to temperature and humidity monitoring. Brought to you by the data logger experts at Dickson.
---

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# audits

## [Food Plants & Warehouses Are Increasingly Being Audited And Fined By The FDA](https://info.dicksondata.com/blog/how-food-plants-and-warehouses-can-prepare-for-an-fda-audit-in-2021-dickson)

[Leave a Comment](https://info.dicksondata.com/blog/how-food-plants-and-warehouses-can-prepare-for-an-fda-audit-in-2021-dickson#comments-listing)  / [Food](https://info.dicksondata.com/blog/tag/food-2), [Environmental Monitoring](https://info.dicksondata.com/blog/tag/environmental-monitoring), [Audits](https://info.dicksondata.com/blog/tag/audits)

Food plants and warehouses have a responsibility to comply with FDA regulations to ensure that high quality products are being distributed to the public. Recently, the FDA has been particularly concerned about temperature monitoring conditions, and therefore, are issuing citations to facilities for...

[Read More](https://info.dicksondata.com/blog/how-food-plants-and-warehouses-can-prepare-for-an-fda-audit-in-2021-dickson)

[![](https://info.dicksondata.com/hubfs/young-focused-female-worker-sterile-clothes-checking-productivity-production-line-food-factory.jpg)](https://info.dicksondata.com/blog/how-food-plants-and-warehouses-can-prepare-for-an-fda-audit-in-2021-dickson) [Sep 30 2021](https://info.dicksondata.com/blog/how-food-plants-and-warehouses-can-prepare-for-an-fda-audit-in-2021-dickson)

## [Preparing For the Return of FDA Surveillance Inspections: A Guide for Pharmaceutical Manufacturers](https://info.dicksondata.com/blog/a-guide-for-successfully-passing-fda-audits-as-they-return-in-2021)

[Leave a Comment](https://info.dicksondata.com/blog/a-guide-for-successfully-passing-fda-audits-as-they-return-in-2021#comments-listing)  / [Pharmaceuticals](https://info.dicksondata.com/blog/tag/pharmaceuticals), [Environmental Monitoring](https://info.dicksondata.com/blog/tag/environmental-monitoring), [Audits](https://info.dicksondata.com/blog/tag/audits), [GMP](https://info.dicksondata.com/blog/tag/gmp)

In July, acting FDA commissioner Janet Woodcock [announced](https://endpts.com/fdas-domestic-biopharma-inspections-return-to-normal-as-agency-faces-backlog-of-8000/) that the FDA would be resuming non-mission-critical facility inspections, [effective immediately](https://www.fiercepharma.com/pharma/restrictions-lifted-fda-free-to-resume-inspections-and-whittle-its-backlog-u-s-at-least). In this article, we’re going to discuss what that means for pharmaceutical companies, and how they can prepare for a successful audit.   

[Read More](https://info.dicksondata.com/blog/a-guide-for-successfully-passing-fda-audits-as-they-return-in-2021)

[![](https://info.dicksondata.com/hubfs/stacks-documents-files-with-black-clip.jpg)](https://info.dicksondata.com/blog/a-guide-for-successfully-passing-fda-audits-as-they-return-in-2021) [Sep 01 2021](https://info.dicksondata.com/blog/a-guide-for-successfully-passing-fda-audits-as-they-return-in-2021)

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