Pharmaceutical Manufacturing Research Services, Inc.

FDA inspection history in Horsham, Pennsylvania, 2015 to 2017

2
Form 483s

Every document, by year

  • Form 483

2015: one Form 483; 2017: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2015–17Two Form 483s, at Horsham, Pennsylvania.
  2. 2017The longest 483 on file: 1 observation over 2 pages at Horsham, Pennsylvania.

Cited most

Across all Pharmaceutical Manufacturing Research Services observations on file

The complete Pharmaceutical Manufacturing Research Services file.

All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$198

The price of the documents, added to your cart together

Sites

Documents

2 on file, newest first
DateDocumentPrice
2017-05-25483 Form 483$99
2015-01-20483 Form 483$99

FEI number 3004752030 · most recent document May 25, 2017

About Pharmaceutical Manufacturing Research Services, Inc.

How many FDA Form 483s has Pharmaceutical Manufacturing Research Services, Inc. received?

FDA Intel has 2 Form 483s on file for Pharmaceutical Manufacturing Research Services, Inc.; the most recent is dated May 25, 2017.

When was Pharmaceutical Manufacturing Research Services, Inc. last inspected by FDA?

The most recent FDA inspection document on file for Pharmaceutical Manufacturing Research Services, Inc. is a Form 483 dated May 25, 2017, for the site in Horsham, Pennsylvania.

What did FDA cite at Pharmaceutical Manufacturing Research Services, Inc.?

The regulations cited most in the observations on file for Pharmaceutical Manufacturing Research Services, Inc. are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.165 (Testing and release for distribution), 1 time.