# Glatt Pharmaceutical Services GmbH & Co. KG - Inspection Records

Source: https://www.keypedia.com/companies/glatt-pharmaceutical-services-gmbh-co-kg/50c9bfb9-5534-47d8-9b08-f29b8953c9df

> Inspection records and compliance data for Glatt Pharmaceutical Services GmbH & Co. KG in Binzen, None. Access full analysis and detailed observations.

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## Details

- Name: Glatt Pharmaceutical Services GmbH & Co. KG
- FEI Number: 3004146501
- City: Binzen
- State: None
- Country Name: Germany
- Address Line 1: Werner-Glatt-Str. 1
- Zip Code: None
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE

## Related Documents

- [FDA Inspection 1271023 - Glatt Pharmaceutical Services GmbH & Co. KG - 2024-04-16](https://www.keypedia.com/records/fda_inspections/glatt-pharmaceutical-services-gmbh-co-kg/d436f249-6774-42b3-8a37-a5af09a5be72) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 16, 2024
- [FDA Inspection 1077899 - Glatt Pharmaceutical Services GmbH & Co. KG - 2018-12-20](https://www.keypedia.com/records/fda_inspections/glatt-pharmaceutical-services-gmbh-co-kg/f656a879-63a6-4127-98aa-f77861223788) — classification: No Action Indicated (NAI), source: FDA, date: December 20, 2018
- [FDA Inspection 935852 - Glatt Pharmaceutical Services GmbH & Co. KG - 2015-07-30](https://www.keypedia.com/records/fda_inspections/glatt-pharmaceutical-services-gmbh-co-kg/6767763e-f13b-464d-9ce4-c3bcd417ecac) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 30, 2015
- [FDA Inspection 850997 - Glatt Pharmaceutical Services GmbH & Co. KG - 2013-09-17](https://www.keypedia.com/records/fda_inspections/glatt-pharmaceutical-services-gmbh-co-kg/393babf0-be5b-4054-b1b5-273b41827d09) — classification: No Action Indicated (NAI), source: FDA, date: September 17, 2013
- [FDA Inspection 635437 - Glatt Pharmaceutical Services GmbH & Co. KG - 2009-12-04](https://www.keypedia.com/records/fda_inspections/glatt-pharmaceutical-services-gmbh-co-kg/ebb70cf8-9cb0-4752-afd0-d0ff3c6fe528) — classification: No Action Indicated (NAI), source: FDA, date: December 4, 2009

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