# Noah W. Kreider & Sons, LLP - Inspection Records

Source: https://www.keypedia.com/companies/noah-w-kreider-sons-llp/c0a8835f-0cec-49ef-ab4b-5d28e388afdb

> Inspection records and compliance data for Noah W. Kreider & Sons, LLP in Manheim, Pennsylvania. Access full analysis and detailed observations.

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## Details

- Name: Noah W. Kreider & Sons, LLP
- FEI Number: 3004325764
- City: Manheim
- State: Pennsylvania
- Country Name: United States
- Address Line 1: 286 Doe Run Rd
- Zip Code: 17545

## Related Documents

- [FDA Inspection 1226657 - Noah W. Kreider & Sons, LLP - 2024-01-03](https://www.keypedia.com/records/fda_inspections/noah-w-kreider-sons-llp/ab4a716b-4511-4c58-bd34-e48883698574) — classification: No Action Indicated (NAI), source: FDA, date: January 3, 2024
- [FDA Inspection 1226657 - Noah W. Kreider & Sons, LLP - 2024-01-03](https://www.keypedia.com/records/fda_inspections/noah-w-kreider-sons-llp/e418cd29-f153-408a-84f1-c3178a5ec2e4) — classification: No Action Indicated (NAI), source: FDA, date: January 3, 2024
- [FDA Inspection 1029236 - Noah W. Kreider & Sons, LLP - 2017-08-01](https://www.keypedia.com/records/fda_inspections/noah-w-kreider-sons-llp/e5e0ee0e-a62b-4f82-a13e-40b172549a42) — classification: No Action Indicated (NAI), source: FDA, date: August 1, 2017
- [FDA Inspection 985400 - Noah W. Kreider & Sons, LLP - 2016-08-09](https://www.keypedia.com/records/fda_inspections/noah-w-kreider-sons-llp/1da93f6c-9ea3-4f34-bdfb-232c646f69d0) — classification: No Action Indicated (NAI), source: FDA, date: August 9, 2016
- [FDA Inspection 767722 - Noah W. Kreider & Sons, LLP - 2012-02-07](https://www.keypedia.com/records/fda_inspections/noah-w-kreider-sons-llp/4cafecd3-d131-48cd-8b24-4e844352a4a2) — classification: No Action Indicated (NAI), source: FDA, date: February 7, 2012
- [FDA Inspection 588282 - Noah W. Kreider & Sons, LLP - 2009-06-11](https://www.keypedia.com/records/fda_inspections/noah-w-kreider-sons-llp/044be8e4-a790-4e15-9f5e-425e144ee573) — classification: No Action Indicated (NAI), source: FDA, date: June 11, 2009

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