FDA Investigator: Liatte Krueger

- Liatte Krueger first started conducting FDA inspections in 2009, with the last inspection in 2016. Over that time, Liatte Krueger has conducted 84 inspections at 80 companies across 83 sites.

Get Liatte Krueger's official FDA inspection documents. Gain valuable insights from their Form 483s and EIRs to ace your next inspection.

Documents

Upon purchase, you will receive an email with a link to immediately download the documents.

FDA 483 Vetter Pharma Fertigung GmbH & Co. KG, Langenargen | 2016

Out-of-stock
Liatte Krueger
Human Drug Form 483

FDA 483 Assia Chemical Industries Ltd - Teva Tech Site, Be'er Sheva | 2016

Out-of-stock
Liatte Krueger
Human Drug Form 483

FDA 483 Forest Research Institute Inc, Jersey City | 2016

Out-of-stock
Liatte Krueger
Human Drug Form 483

FDA 483 Elite Laboratories Inc., Northvale | 2016

Out-of-stock
Liatte Krueger
Human Drug Form 483

FDA 483 5N Plus Lubeck GmbH, Lubeck | 2015

Out-of-stock
Liatte Krueger
Human Drug Form 483

FDA 483 Glatt GmbH, Binzen | 2015

Out-of-stock
Liatte Krueger
Human Drug Form 483

FDA 483 Procter & Gamble Mfg. Gmbh, Gros-Gerau | 2015

Out-of-stock
Liatte Krueger
Human Drug Form 483

FDA 483 Millers of Wyckoff, Inc., Wyckoff | 2015

Out-of-stock
Liatte Krueger
Human Drug Form 483

FDA 483 Sun Pharmaceutical Industries, Inc., Cranbury | 2015

Out-of-stock
Liatte Krueger
Human Drug Form 483

FDA 483 Novartis Pharmaceuticals Corp., East Hanover | 2015

Out-of-stock
Liatte Krueger
Human Drug Form 483

FDA 483 Micra Biotechnologies, Inc., River Edge | 2015

Out-of-stock
Liatte Krueger
Human Drug Form 483

FDA 483 Egis PLC, Budapest | 2014

Out-of-stock
Liatte Krueger
Human Drug Form 483