Hill-Rom, Inc.
FDA inspection history in Batesville, Indiana, 2013 to 2015
- 1
- Close-out
- 1
- Form 483
Every document, by year
- Close-out
- Form 483
2013: one Form 483; 2015: one close-out letter.
The story so far
Built from the dates and citations on the documents themselves.
- 2013–15One Form 483 and one close-out letter, at Batesville, Indiana.
Cited most
Across all Hill-Rom observations on file
- 21 CFR 820.30(f)Design controls5
- 21 CFR 820.60Identification2
- 21 CFR 8201
- 21 CFR 803.17What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?1
- 21 CFR 820.198(c)Complaint files1
The complete Hill-Rom file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Batesville, Indiana
One close-out letter and one Form 483 · 2013 to 2015 · 11 observations
Latest: Close-out, Sep 10, 2015 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-09-10 | Close-out Close-out letter | Batesville, Indiana | — | $99 |
| 2013-01-11 | 483 Form 483 | Batesville, Indiana | 11 | $99 |
Investigators on these documents
Joseph R. Strelnik (1)Patrick B. Cummings (1)Sean T. Creighton (1)
FEI number 1824206 · most recent document Sep 10, 2015
About Hill-Rom, Inc.
How many FDA Form 483s has Hill-Rom, Inc. received?
FDA Intel has 1 Form 483 on file for Hill-Rom, Inc.; the most recent is dated Jan 11, 2013.
When was Hill-Rom, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Hill-Rom, Inc. is a Form 483 dated Jan 11, 2013, for the site in Batesville, Indiana.
What did FDA cite at Hill-Rom, Inc.?
The regulations cited most in the observations on file for Hill-Rom, Inc. are 21 CFR 820.30(f) (Design controls), 5 times; 21 CFR 820.60 (Identification), 2 times; 21 CFR 820, 1 time.